Canonical Allele Identifier: CA2273295120
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70831959A= , CM000679.2:g.70831959A= GRCh38
NC_000017.10:g.68828100A= , CM000679.1:g.68828100A= GRCh37
NC_000017.9:g.66339695A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934956.1:n.62+3255T=
XR_934956.2:n.114+3255T=