Canonical Allele Identifier: CA879416188

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8945785T>A , CM000685.2:g.8945785T>A	GRCh38
NC_000023.10:g.8913826T>A , CM000685.1:g.8913826T>A	GRCh37
NC_000023.9:g.8873826T>A	NCBI36