Canonical Allele Identifier: CA1980170025
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482969A= , CM000673.2:g.67482969A= GRCh38
NC_000011.9:g.67250440A= , CM000673.1:g.67250440A= GRCh37
NC_000011.8:g.67007016A= NCBI36
NG_008969.1:g.4936A= , LRG_460:g.4936A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-190A= ENSP00000507935.1:n.-190A=
XM_024448761.1:c.-190A= XP_024304529.1:n.-190A=