Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.10756840T>C	CA5884894	CTR9	c.592+2T>C (n.592+2T>C) c.553+2T>C (n.553+2T>C)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11	g.10756840T=	CA1952039726	CTR9	c.592+2T= (n.592+2T=) c.553+2T= (n.553+2T=)	dbSNP

Number of alleles fetched