Canonical Allele Identifier: CA1817437352

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125474219T= , CM000670.2:g.125474219T=	GRCh38
NC_000008.10:g.126486461T= , CM000670.1:g.126486461T=	GRCh37
NC_000008.9:g.126555643T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+905T=