Canonical Allele Identifier: CA1596629102

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656532G= , CM000667.2:g.162656532G=	GRCh38
NC_000005.9:g.162083538G= , CM000667.1:g.162083538G=	GRCh37
NC_000005.8:g.162016116G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3570C=