Canonical Allele Identifier: CA2267413169
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788794G= , CM000679.2:g.57788794G= GRCh38
NC_000017.10:g.55866155G= , CM000679.1:g.55866155G= GRCh37
NC_000017.9:g.53221154G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934881.1:n.1608-16598C=
XR_934881.3:n.3815-16598C=