Canonical Allele Identifier: CA2206404259
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249658G= , CM000678.2:g.9249658G= GRCh38
NC_000016.9:g.9343515G= , CM000678.1:g.9343515G= GRCh37
NC_000016.8:g.9251016G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64925G=