Canonical Allele Identifier: CA1502607239

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148748354T= , CM000666.2:g.148748354T=	GRCh38
NC_000004.11:g.149669506T= , CM000666.1:g.149669506T=	GRCh37
NC_000004.10:g.149888956T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741441.1:n.1746-118403T=