Canonical Allele Identifier: CA197846305
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs12236285

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092962G>A , CM000671.2:g.108092962G>A GRCh38
NC_000009.11:g.110855243G>A , CM000671.1:g.110855243G>A GRCh37
NC_000009.10:g.109895064G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-39668C>T
XR_001746881.1:n.668-39668C>T
XR_001746882.1:n.668-39668C>T