Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5226976A>C	CA125124	HBB	c.46T>G (p.Trp16Gly) n.97T>G	ClinVar dbSNP
11	g.5226976A>G	CA217115404	HBB	c.46T>C (p.Trp16Arg) n.97T>C	dbSNP
11	g.5226976A>T	CA124742	HBB	c.46T>A (p.Trp16Arg) n.97T>A	ClinVar dbSNP

Number of alleles fetched