Canonical Allele Identifier: CA689655492

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50486433T>A , CM000674.2:g.50486433T>A	GRCh38
NC_000012.11:g.50880216T>A , CM000674.1:g.50880216T>A	GRCh37
NC_000012.10:g.49166483T>A	NCBI36