Canonical Allele Identifier: CA2614617881
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483011G>A , CM000673.2:g.67483011G>A GRCh38
NC_000011.9:g.67250482G>A , CM000673.1:g.67250482G>A GRCh37
NC_000011.8:g.67007058G>A NCBI36
NG_008969.1:g.4978G>A , LRG_460:g.4978G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-148G>A ENSP00000507935.1:n.-148G>A
XM_024448761.1:c.-148G>A XP_024304529.1:n.-148G>A