Canonical Allele Identifier: CA1769514553

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20734955C= , CM000670.2:g.20734955C=	GRCh38
NC_000008.10:g.20592466C= , CM000670.1:g.20592466C=	GRCh37
NC_000008.9:g.20636746C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949569.3:n.72-55491C=