Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
10	g.52771466C>T	CA123881	MBL2	c.170G>A (p.Gly57Glu)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10	g.52771466C=	CA1910259311	MBL2	c.170G= (p.Gly57=)	dbSNP
10	g.52771466C>G	CA376539990	MBL2	c.170G>C (p.Gly57Ala)	dbSNP gnomAD v4

Number of alleles fetched