Canonical Allele Identifier: CA2144442981

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68743482G= , CM000676.2:g.68743482G=	GRCh38
NC_000014.8:g.69210199G= , CM000676.1:g.69210199G=	GRCh37
NC_000014.7:g.68279952G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001750931.1:n.376-895C=