Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5226995C>T	CA472885719	HBB	c.27G>A (p.Lys9=) n.78G>A	ClinVar dbSNP gnomAD v3 gnomAD v4
11	g.5226995C>G	CA125503	HBB	c.27G>C (p.Lys9Asn) n.78G>C	ClinVar dbSNP COSMIC

Number of alleles fetched