Canonical Allele Identifier: CA770885509

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60696885A>T , CM000664.2:g.60696885A>T	GRCh38
NC_000002.11:g.60924020A>T , CM000664.1:g.60924020A>T	GRCh37
NC_000002.10:g.60777524A>T	NCBI36