Canonical Allele Identifier: CA2720283646
Gene:

Linked Data

dbSNP Id: rs2118594203

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092895C>A , CM000671.2:g.108092895C>A GRCh38
NC_000009.11:g.110855176C>A , CM000671.1:g.110855176C>A GRCh37
NC_000009.10:g.109894997C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-39601G>T
XR_001746881.1:n.668-39601G>T
XR_001746882.1:n.668-39601G>T