Canonical Allele Identifier: CA2206404198

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249543G= , CM000678.2:g.9249543G=	GRCh38
NC_000016.9:g.9343400G= , CM000678.1:g.9343400G=	GRCh37
NC_000016.8:g.9250901G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64810G=