Canonical Allele Identifier: CA1889344497

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697526C= , CM000672.2:g.8697526C=	GRCh38
NC_000010.10:g.8739489C= , CM000672.1:g.8739489C=	GRCh37
NC_000010.9:g.8779495C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27725G=