Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5234385C>T	CA379277258	HBD	c.49G>A (p.Gly17Ser)	dbSNP COSMIC
11	g.5234385C>G	CA124633	HBD	c.49G>C (p.Gly17Arg)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11	g.5234385C=	CA1949565805	HBD	c.49G= (p.Gly17=)	dbSNP

Number of alleles fetched