Canonical Allele Identifier: CA2614627858
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67491110-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491110T>A , CM000673.2:g.67491110T>A GRCh38
NC_000011.9:g.67258581T>A , CM000673.1:g.67258581T>A GRCh37
NC_000011.8:g.67015157T>A NCBI36
NG_008969.1:g.13077T>A , LRG_460:g.13077T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*117T>A ENSP00000507961.1:n.*117T>A
Search 100 bp 5'
Search 100 bp 3'