Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5226957T>C	CA124805	HBB	c.65A>G (p.Asp22Gly) n.116A>G	ClinVar dbSNP
11	g.5226957T>A	CA217115275	HBB	c.65A>T (p.Asp22Val) n.116A>T	ClinVar dbSNP

Number of alleles fetched