Canonical Allele Identifier: CA885736793

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113761093G>A , CM000663.2:g.113761093G>A	GRCh38
NC_000001.10:g.114303715G>A , CM000663.1:g.114303715G>A	GRCh37
NC_000001.9:g.114105238G>A	NCBI36