Canonical Allele Identifier: CA1980170057
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483022C= , CM000673.2:g.67483022C= GRCh38
NC_000011.9:g.67250493C= , CM000673.1:g.67250493C= GRCh37
NC_000011.8:g.67007069C= NCBI36
NG_008969.1:g.4989C= , LRG_460:g.4989C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-137C= ENSP00000507935.1:n.-137C=
XM_024448761.1:c.-137C= XP_024304529.1:n.-137C=