Canonical Allele Identifier: CA1374121566

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.72266805T= , CM000665.2:g.72266805T=	GRCh38
NC_000003.11:g.72315956T= , CM000665.1:g.72315956T=	GRCh37
NC_000003.10:g.72398646T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940958.1:n.835+8303A=