Canonical Allele Identifier: CA2002397712
Gene:

Linked Data

dbSNP Id: rs1864209265

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072470C>A , CM000673.2:g.116072470C>A GRCh38
NC_000011.9:g.115943188C>A , CM000673.1:g.115943188C>A GRCh37
NC_000011.8:g.115448398C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+544G>T
XR_948056.1:n.311-5265G>T
XR_948057.1:n.97+639G>T
XR_001748401.1:n.192+544G>T
XR_948055.2:n.192+544G>T
XR_948056.2:n.314-5265G>T
XR_948057.2:n.97+639G>T