Canonical Allele Identifier: CA1704517819

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.46033036T= , CM000669.2:g.46033036T=	GRCh38
NC_000007.13:g.46072634T= , CM000669.1:g.46072634T=	GRCh37
NC_000007.12:g.46039159T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745203.1:n.1270-3582T=