Canonical Allele Identifier: CA1980170058
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483024G= , CM000673.2:g.67483024G= GRCh38
NC_000011.9:g.67250495G= , CM000673.1:g.67250495G= GRCh37
NC_000011.8:g.67007071G= NCBI36
NG_008969.1:g.4991G= , LRG_460:g.4991G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-135G= ENSP00000507935.1:n.-135G=
XM_024448761.1:c.-135G= XP_024304529.1:n.-135G=