Canonical Allele Identifier: CA2263926986
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211860T= , CM000679.2:g.50211860T= GRCh38
NC_000017.10:g.48289221T= , CM000679.1:g.48289221T= GRCh37
NC_000017.9:g.45644220T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-1975T=