Canonical Allele Identifier: CA2614627958
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491133G>A , CM000673.2:g.67491133G>A GRCh38
NC_000011.9:g.67258604G>A , CM000673.1:g.67258604G>A GRCh37
NC_000011.8:g.67015180G>A NCBI36
NG_008969.1:g.13100G>A , LRG_460:g.13100G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*140G>A ENSP00000507961.1:n.*140G>A