Canonical Allele Identifier: CA780112016

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49655298A>G , CM000680.2:g.49655298A>G	GRCh38
NC_000018.9:g.47181668A>G , CM000680.1:g.47181668A>G	GRCh37
NC_000018.8:g.45435666A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935461.1:n.162-6736A>G
XR_001753446.1:n.898-6736A>G