Canonical Allele Identifier: CA212166521
Gene:

Linked Data

dbSNP Id: rs901129991

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750673G>A , CM000672.2:g.101750673G>A GRCh38
NC_000010.10:g.103510430G>A , CM000672.1:g.103510430G>A GRCh37
NC_000010.9:g.103500420G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946255.1:n.217-6456C>T
XR_946255.2:n.217-6456C>T