Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5250053G>A	CA124626	HBG2	c.316-1566C>T (n.316-1566C>T) c.379-1566C>T (n.379-1566C>T)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11	g.5250053G=	CA1949584387	HBG2	c.316-1566C= (n.316-1566C=) c.379-1566C= (n.379-1566C=)	dbSNP

Number of alleles fetched