Canonical Allele Identifier: CA2206394093
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9232128C>A , CM000678.2:g.9232128C>A GRCh38
NC_000016.9:g.9325985C>A , CM000678.1:g.9325985C>A GRCh37
NC_000016.8:g.9233486C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+47395C>A