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Chromosome 19 - NC_000019.10
Genomic Sequence: NC_000019.10 Chromosome 19 Reference GRCh38.p14 Primary Assembly NW_003571054.1 Chromosome 19 Reference GRCh38.p14 ALT_REF_LOCI_1 NW_003571055.2 Chromosome 19 Reference GRCh38.p14 ALT_REF_LOCI_2 NW_003571056.2 Chromosome 19 Reference GRCh38.p14 ALT_REF_LOCI_3 NW_003571057.2 Chromosome 19 Reference GRCh38.p14 ALT_REF_LOCI_4 NW_003571058.2 Chromosome 19 Reference GRCh38.p14 ALT_REF_LOCI_5 NW_003571059.2 Chromosome 19 Reference GRCh38.p14 ALT_REF_LOCI_6 NW_003571060.1 Chromosome 19 Reference GRCh38.p14 ALT_REF_LOCI_7 NW_003571061.2 Chromosome 19 Reference GRCh38.p14 ALT_REF_LOCI_8 NT_187693.1 Chromosome 19 Reference GRCh38.p14 ALT_REF_LOCI_9 NC_060943.1 Chromosome 19 Alternate T2T-CHM13v2.0 NC_000019.9 Chromosome 19 Reference GRCh37.p13 Primary Assembly NW_003571054.1 Chromosome 19 Reference GRCh37.p13 PATCHES NW_003571055.1 Chromosome 19 Reference GRCh37.p13 PATCHES NW_003571056.1 Chromosome 19 Reference GRCh37.p13 PATCHES NW_003571057.1 Chromosome 19 Reference GRCh37.p13 PATCHES NW_003571058.1 Chromosome 19 Reference GRCh37.p13 PATCHES NW_003571059.1 Chromosome 19 Reference GRCh37.p13 PATCHES NW_003571060.1 Chromosome 19 Reference GRCh37.p13 PATCHES NW_003571061.1 Chromosome 19 Reference GRCh37.p13 PATCHES NW_004166865.1 Chromosome 19 Reference GRCh37.p13 PATCHES
Go to nucleotide: Graphics FASTA GenBank
See all (44) citations in PubMed
Review eQTL and phenotype association data in this region using PheGenI
See variants in ClinVar
See studies and variants in dbVar
See Variation Viewer (GRCh37.p13)
See Variation Viewer (GRCh38)
NEW Try the new Transcript table
These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.
NM_001321792.2 → NP_001308721.1 TCF3 fusion partner isoform 2
Status: VALIDATED
NM_013342.4 → NP_037474.1 TCF3 fusion partner isoform 1
See identical proteins and their annotated locations for NP_037474.1
The following sections contain reference sequences that belong to a specific genome build. Explain
This section includes genomic Reference Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate assemblies. Model RNAs and proteins are also reported here.
NC_000019.10 Reference GRCh38.p14 Primary Assembly
XM_005278261.2 → XP_005278318.1 TCF3 fusion partner isoform X1
See identical proteins and their annotated locations for XP_005278318.1
NW_003571054.1 Reference GRCh38.p14 ALT_REF_LOCI_1
XM_054329680.1 → XP_054185655.1 TCF3 fusion partner isoform X1
NW_003571055.2 Reference GRCh38.p14 ALT_REF_LOCI_2
XM_054330165.1 → XP_054186140.1 TCF3 fusion partner isoform X1
NW_003571056.2 Reference GRCh38.p14 ALT_REF_LOCI_3
XM_054330473.1 → XP_054186448.1 TCF3 fusion partner isoform X1
NW_003571057.2 Reference GRCh38.p14 ALT_REF_LOCI_4
XM_054330726.1 → XP_054186701.1 TCF3 fusion partner isoform X1
NW_003571058.2 Reference GRCh38.p14 ALT_REF_LOCI_5
XM_054330955.1 → XP_054186930.1 TCF3 fusion partner isoform X1
NW_003571059.2 Reference GRCh38.p14 ALT_REF_LOCI_6
XM_054331235.1 → XP_054187210.1 TCF3 fusion partner isoform X1
NW_003571060.1 Reference GRCh38.p14 ALT_REF_LOCI_7
XM_054331510.1 → XP_054187485.1 TCF3 fusion partner isoform X1
NW_003571061.2 Reference GRCh38.p14 ALT_REF_LOCI_8
XM_054333545.1 → XP_054189520.1 TCF3 fusion partner isoform X1
NT_187693.1 Reference GRCh38.p14 ALT_REF_LOCI_9
XM_054333646.1 → XP_054189621.1 TCF3 fusion partner isoform X1
NC_060943.1 Alternate T2T-CHM13v2.0
XM_054320762.1 → XP_054176737.1 TCF3 fusion partner isoform X1
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