Canonical Allele Identifier: CA2835839432
Gene: AIP HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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