Canonical Allele Identifier: CA2809958345
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788779C>T , CM000679.2:g.57788779C>T GRCh38
NC_000017.10:g.55866140C>T , CM000679.1:g.55866140C>T GRCh37
NC_000017.9:g.53221139C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934881.1:n.1608-16583G>A
XR_934881.3:n.3815-16583G>A