Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5226988C>A	CA125412	HBB	c.34G>T (p.Val12Phe) n.85G>T	ClinVar dbSNP
11	g.5226988C>T	CA124888	HBB	c.34G>A (p.Val12Ile) n.85G>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched