Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5226990G>T	CA124726	HBB	c.32C>A (p.Ala11Asp) n.83C>A	ClinVar dbSNP
11	g.5226990G>A	CA125466	HBB	c.32C>T (p.Ala11Val) n.83C>T	ClinVar dbSNP gnomAD v4
11	g.5226990G=	CA1949570892	HBB	c.32C= (p.Ala11=) n.83C=	dbSNP

Number of alleles fetched