Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.46011053G>T	CA9886461	MMP9	c.649+3G>T (n.649+3G>T)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20	g.46011053G=	CA2366478591	MMP9	c.649+3G= (n.649+3G=)	dbSNP

Number of alleles fetched