Canonical Allele Identifier: CA2263926958
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211800G= , CM000679.2:g.50211800G= GRCh38
NC_000017.10:g.48289161G= , CM000679.1:g.48289161G= GRCh37
NC_000017.9:g.45644160G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2035G=