Canonical Allele Identifier: CA1818149606

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.126999601T= , CM000670.2:g.126999601T=	GRCh38
NC_000008.10:g.128011846T= , CM000670.1:g.128011846T=	GRCh37
NC_000008.9:g.128081028T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746076.2:n.1301-6954T=