Canonical Allele Identifier: CA690217323

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56661507C>G , CM000674.2:g.56661507C>G	GRCh38
NC_000012.11:g.57055291C>G , CM000674.1:g.57055291C>G	GRCh37
NC_000012.10:g.55341558C>G	NCBI36