Canonical Allele Identifier: CA786695499
Gene:

Linked Data

dbSNP Id: rs1214660973

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578033G>A , CM000666.2:g.12578033G>A GRCh38
NC_000004.11:g.12579657G>A , CM000666.1:g.12579657G>A GRCh37
NC_000004.10:g.12188755G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31309C>T
XR_001741374.1:n.254+44622C>T
XR_925406.3:n.140+31309C>T