Canonical Allele Identifier: CA1980170020
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482961C= , CM000673.2:g.67482961C= GRCh38
NC_000011.9:g.67250432C= , CM000673.1:g.67250432C= GRCh37
NC_000011.8:g.67007008C= NCBI36
NG_008969.1:g.4928C= , LRG_460:g.4928C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-198C= ENSP00000507935.1:n.-198C=
XM_024448761.1:c.-198C= XP_024304529.1:n.-198C=