Canonical Allele Identifier: CA1769514538
Gene:

Linked Data

dbSNP Id: rs1799796165

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734933A>G , CM000670.2:g.20734933A>G GRCh38
NC_000008.10:g.20592444A>G , CM000670.1:g.20592444A>G GRCh37
NC_000008.9:g.20636724A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55513A>G