Canonical Allele Identifier: CA2263927014
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211912T= , CM000679.2:g.50211912T= GRCh38
NC_000017.10:g.48289273T= , CM000679.1:g.48289273T= GRCh37
NC_000017.9:g.45644272T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-1923T=