Canonical Allele Identifier: CA2263926877
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211614C= , CM000679.2:g.50211614C= GRCh38
NC_000017.10:g.48288975C= , CM000679.1:g.48288975C= GRCh37
NC_000017.9:g.45643974C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.42+2208C=