Canonical Allele Identifier: CA884596189

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.101414449T>A , CM000663.2:g.101414449T>A	GRCh38
NC_000001.10:g.101880005T>A , CM000663.1:g.101880005T>A	GRCh37
NC_000001.9:g.101652593T>A	NCBI36