Canonical Allele Identifier: CA2614617631
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67482961-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482961C>A , CM000673.2:g.67482961C>A GRCh38
NC_000011.9:g.67250432C>A , CM000673.1:g.67250432C>A GRCh37
NC_000011.8:g.67007008C>A NCBI36
NG_008969.1:g.4928C>A , LRG_460:g.4928C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-198C>A ENSP00000507935.1:n.-198C>A
XM_024448761.1:c.-198C>A XP_024304529.1:n.-198C>A
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