Canonical Allele Identifier: CA2273295137
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70831994T= , CM000679.2:g.70831994T= GRCh38
NC_000017.10:g.68828135T= , CM000679.1:g.68828135T= GRCh37
NC_000017.9:g.66339730T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934956.1:n.62+3220A=
XR_934956.2:n.114+3220A=