Canonical Allele Identifier: CA2614617495
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482939G>T , CM000673.2:g.67482939G>T GRCh38
NC_000011.9:g.67250410G>T , CM000673.1:g.67250410G>T GRCh37
NC_000011.8:g.67006986G>T NCBI36
NG_008969.1:g.4906G>T , LRG_460:g.4906G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-220G>T ENSP00000507935.1:n.-220G>T
XM_024448761.1:c.-220G>T XP_024304529.1:n.-220G>T