Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
9	g.136676603G>T	CA277952	AGPAT2	c.570C>A (p.Tyr190Ter) c.492+358C>A (n.492+358C>A) n.498C>A	ClinVar dbSNP gnomAD v3 gnomAD v4
9	g.136676603G>A	CA5342938	AGPAT2	c.570C>T (p.Tyr190=) c.492+358C>T (n.492+358C>T) n.498C>T	dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched