Canonical Allele Identifier: CA2614617667
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482967A>C , CM000673.2:g.67482967A>C GRCh38
NC_000011.9:g.67250438A>C , CM000673.1:g.67250438A>C GRCh37
NC_000011.8:g.67007014A>C NCBI36
NG_008969.1:g.4934A>C , LRG_460:g.4934A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-192A>C ENSP00000507935.1:n.-192A>C
XM_024448761.1:c.-192A>C XP_024304529.1:n.-192A>C