Canonical Allele Identifier: CA281734263
Gene:

Linked Data

dbSNP Id: rs1362756

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51424379C>G , CM000678.2:g.51424379C>G GRCh38
NC_000016.9:g.51458290C>G , CM000678.1:g.51458290C>G GRCh37
NC_000016.8:g.50015791C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_933554.1:n.926-19751G>C
XR_933558.1:n.856-19751G>C
XR_933554.2:n.1262-19751G>C
XR_933558.2:n.1192-19751G>C