Canonical Allele Identifier: CA1596629171

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656594T= , CM000667.2:g.162656594T=	GRCh38
NC_000005.9:g.162083600T= , CM000667.1:g.162083600T=	GRCh37
NC_000005.8:g.162016178T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3508A=