Canonical Allele Identifier: CA669972877

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92705706G>A , CM000672.2:g.92705706G>A	GRCh38
NC_000010.10:g.94465463G>A , CM000672.1:g.94465463G>A	GRCh37
NC_000010.9:g.94455443G>A	NCBI36