Canonical Allele Identifier: CA2002576374

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116442774C= , CM000673.2:g.116442774C=	GRCh38
NC_000011.9:g.116313491C= , CM000673.1:g.116313491C=	GRCh37
NC_000011.8:g.115818701C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001748403.1:n.349+31103G=