Canonical Allele Identifier: CA1889344482

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697491T= , CM000672.2:g.8697491T=	GRCh38
NC_000010.10:g.8739454T= , CM000672.1:g.8739454T=	GRCh37
NC_000010.9:g.8779460T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27690A=