Canonical Allele Identifier: CA1818161699

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127012527T= , CM000670.2:g.127012527T=	GRCh38
NC_000008.10:g.128024772T= , CM000670.1:g.128024772T=	GRCh37
NC_000008.9:g.128093954T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746076.2:n.1364+5909T=