Canonical Allele Identifier: CA1818149632

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.126999625A= , CM000670.2:g.126999625A=	GRCh38
NC_000008.10:g.128011870A= , CM000670.1:g.128011870A=	GRCh37
NC_000008.9:g.128081052A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001746076.2:n.1301-6930A=