Canonical Allele Identifier: CA16123517
Gene:

Linked Data

dbSNP Id: rs12617311

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767841G>A , CM000664.2:g.198767841G>A GRCh38
NC_000002.11:g.199632565G>A , CM000664.1:g.199632565G>A GRCh37
NC_000002.10:g.199340810G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923758.1:n.72+4418C>T
XR_923759.1:n.72+4418C>T
XR_923760.1:n.72+4418C>T
XR_923759.2:n.72+4418C>T
XR_923760.2:n.72+4418C>T