Canonical Allele Identifier: CA890063415

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159705927T>A , CM000663.2:g.159705927T>A	GRCh38
NC_000001.10:g.159675717T>A , CM000663.1:g.159675717T>A	GRCh37
NC_000001.9:g.157942341T>A	NCBI36