Canonical Allele Identifier: CA229980931
Gene:

Linked Data

dbSNP Id: rs543265329

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072436G>A , CM000673.2:g.116072436G>A GRCh38
NC_000011.9:g.115943154G>A , CM000673.1:g.115943154G>A GRCh37
NC_000011.8:g.115448364G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+578C>T
XR_948056.1:n.311-5231C>T
XR_948057.1:n.97+673C>T
XR_001748401.1:n.192+578C>T
XR_948055.2:n.192+578C>T
XR_948056.2:n.314-5231C>T
XR_948057.2:n.97+673C>T