Canonical Allele Identifier: CA1980170022
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs1303605345

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482964A>C , CM000673.2:g.67482964A>C GRCh38
NC_000011.9:g.67250435A>C , CM000673.1:g.67250435A>C GRCh37
NC_000011.8:g.67007011A>C NCBI36
NG_008969.1:g.4931A>C , LRG_460:g.4931A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-195A>C ENSP00000507935.1:n.-195A>C
XM_024448761.1:c.-195A>C XP_024304529.1:n.-195A>C