Canonical Allele Identifier: CA2614617832
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67482997-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482997A>T , CM000673.2:g.67482997A>T GRCh38
NC_000011.9:g.67250468A>T , CM000673.1:g.67250468A>T GRCh37
NC_000011.8:g.67007044A>T NCBI36
NG_008969.1:g.4964A>T , LRG_460:g.4964A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-162A>T ENSP00000507935.1:n.-162A>T
XM_024448761.1:c.-162A>T XP_024304529.1:n.-162A>T
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