Canonical Allele Identifier: CA942547583
Gene:

Linked Data

dbSNP Id: rs1864210514

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072558G>A , CM000673.2:g.116072558G>A GRCh38
NC_000011.9:g.115943276G>A , CM000673.1:g.115943276G>A GRCh37
NC_000011.8:g.115448486G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+456C>T
XR_948056.1:n.311-5353C>T
XR_948057.1:n.97+551C>T
XR_001748401.1:n.192+456C>T
XR_948055.2:n.192+456C>T
XR_948056.2:n.314-5353C>T
XR_948057.2:n.97+551C>T