Canonical Allele Identifier: CA298296836
Gene:

Linked Data

dbSNP Id: rs115776489

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756465G>A , CM000680.2:g.31756465G>A GRCh38
NC_000018.9:g.29336428G>A , CM000680.1:g.29336428G>A GRCh37
NC_000018.8:g.27590426G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5674G>A