Canonical Allele Identifier: CA1980170021
Gene: AIP HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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