Canonical Allele Identifier: CA889417061

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152469813T>A , CM000663.2:g.152469813T>A	GRCh38
NC_000001.10:g.152442289T>A , CM000663.1:g.152442289T>A	GRCh37
NC_000001.9:g.150708913T>A	NCBI36