Canonical Allele Identifier: CA2614628025
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491142C>G , CM000673.2:g.67491142C>G GRCh38
NC_000011.9:g.67258613C>G , CM000673.1:g.67258613C>G GRCh37
NC_000011.8:g.67015189C>G NCBI36
NG_008969.1:g.13109C>G , LRG_460:g.13109C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*149C>G ENSP00000507961.1:n.*149C>G