Canonical Allele Identifier: CA2614617740
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67482981-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482981A>C , CM000673.2:g.67482981A>C GRCh38
NC_000011.9:g.67250452A>C , CM000673.1:g.67250452A>C GRCh37
NC_000011.8:g.67007028A>C NCBI36
NG_008969.1:g.4948A>C , LRG_460:g.4948A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-178A>C ENSP00000507935.1:n.-178A>C
XM_024448761.1:c.-178A>C XP_024304529.1:n.-178A>C
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