Canonical Allele Identifier: CA927717767
Gene:

Linked Data

dbSNP Id: rs1405722167

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318700G>A , CM000672.2:g.43318700G>A GRCh38
NC_000010.10:g.43814148G>A , CM000672.1:g.43814148G>A GRCh37
NC_000010.9:g.43134154G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+105G>A
XR_945902.2:n.198+105G>A