Canonical Allele Identifier: CA2810939458
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321220C>A , CM000680.2:g.10321220C>A GRCh38
NC_000018.9:g.10321217C>A , CM000680.1:g.10321217C>A GRCh37
NC_000018.8:g.10311217C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+928G>T
XR_001753344.1:n.650+928G>T
XR_001753345.1:n.901G>T
XR_001753346.1:n.549+928G>T