Canonical Allele Identifier: CA1889449088

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.9011169C= , CM000672.2:g.9011169C=	GRCh38
NC_000010.10:g.9053132C= , CM000672.1:g.9053132C=	GRCh37
NC_000010.9:g.9093138C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.32+54194G=