Canonical Allele Identifier: CA2263926955
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211794T= , CM000679.2:g.50211794T= GRCh38
NC_000017.10:g.48289155T= , CM000679.1:g.48289155T= GRCh37
NC_000017.9:g.45644154T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2041T=