Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5226620T>C	CA125132	HBB	c.272A>G (p.Glu91Gly) c.272A>G n.204A>G n.323A>G c.88A>G (n.88A>G)	ClinVar dbSNP
11	g.5226620T=	CA1949567703	HBB	c.272A= (p.Glu91=) c.272A= n.204A= n.323A= c.88A= (n.88A=)	dbSNP

Number of alleles fetched