Canonical Allele Identifier: CA2259755749
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40890629C>T , CM000679.2:g.40890629C>T GRCh38
NC_000017.10:g.39046881C>T , CM000679.1:g.39046881C>T GRCh37
NC_000017.9:g.36300407C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934754.1:n.1501-27600C>T
XR_934754.2:n.2009-27600C>T