Canonical Allele Identifier: CA694619171

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.105516850C>A , CM000675.2:g.105516850C>A	GRCh38
NC_000013.10:g.106169199C>A , CM000675.1:g.106169199C>A	GRCh37
NC_000013.9:g.104967200C>A	NCBI36