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Chromosome 22 - NC_000022.11
Genomic Sequence: NC_000022.11 Chromosome 22 Reference GRCh38.p14 Primary Assembly NT_187630.1 Chromosome 22 Reference GRCh38.p14 ALT_REF_LOCI_1 NC_060946.1 Chromosome 22 Alternate T2T-CHM13v2.0 NC_000022.10 Chromosome 22 Reference GRCh37.p13 Primary Assembly
Go to nucleotide: Graphics FASTA GenBank
See all (8) citations in PubMed
Find tests for this gene in the NIH Genetic Testing Registry (GTR)
Review eQTL and phenotype association data in this region using PheGenI
See Variation Viewer (GRCh37.p13)
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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_030642.1 → NP_085145.1 apolipoprotein L5
See identical proteins and their annotated locations for NP_085145.1
Status: REVIEWED
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_000022.11 Reference GRCh38.p14 Primary Assembly
XM_006724321.5 → XP_006724384.1 apolipoprotein L5 isoform X1
XM_017028945.3 → XP_016884434.1 apolipoprotein L5 isoform X2
NT_187630.1 Reference GRCh38.p14 ALT_REF_LOCI_1
XM_054329449.1 → XP_054185424.1 apolipoprotein L5 isoform X1
XM_054329450.1 → XP_054185425.1 apolipoprotein L5 isoform X2
NC_060946.1 Alternate T2T-CHM13v2.0
XM_054325944.1 → XP_054181919.1 apolipoprotein L5 isoform X1
XM_054325945.1 → XP_054181920.1 apolipoprotein L5 isoform X2
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