Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5226621C>T	CA124716	HBB	c.271G>A (p.Glu91Lys) c.271G>A n.203G>A n.322G>A c.87G>A (n.87G>A)	ClinVar dbSNP gnomAD v4
11	g.5226621C>A	CA125368	HBB	c.271G>T (p.Glu91Ter) c.271G>T n.203G>T n.322G>T c.87G>T (n.87G>T)	ClinVar dbSNP

Number of alleles fetched