Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
19	g.35284804G>A	CA9375792	HAMP	c.106G>A (p.Glu36Lys) n.2288G>A	dbSNP ExAC gnomAD v2 gnomAD v4
19	g.35284804G>C	CA405300549	HAMP	c.106G>C (p.Glu36Gln) n.2288G>C
19	g.35284804G=	CA2333586014	HAMP	c.106G= (p.Glu36=) n.2288G=
19	g.35284804G>T	CA405300552	HAMP	c.106G>T (p.Glu36Ter) n.2288G>T
19	g.35284805A=	CA2333586015	HAMP	c.107A= (p.Glu36=) n.2289A=
19	g.35284805A>C	CA405300556	HAMP	c.107A>C (p.Glu36Ala) n.2289A>C	dbSNP gnomAD v2
19	g.35284805A>G	CA405300562	HAMP	c.107A>G (p.Glu36Gly) n.2289A>G
19	g.35284805A>T	CA405300563	HAMP	c.107A>T (p.Glu36Val) n.2289A>T
19	g.35284806G>A	CA507040991	HAMP	c.108G>A (p.Glu36=) n.2290G>A	ClinVar dbSNP gnomAD v4
19	g.35284806G>C	CA405300567	HAMP	c.108G>C (p.Glu36Asp) n.2290G>C
19	g.35284806G=	CA2333586016	HAMP	c.108G= (p.Glu36=) n.2290G=
19	g.35284806G>T	CA405300570	HAMP	c.108G>T (p.Glu36Asp) n.2290G>T
19	g.35284807C>A	CA405300579	HAMP	c.109C>A (p.Leu37Met) n.2291C>A
19	g.35284807C=	CA2333586017	HAMP	c.109C= (p.Leu37=) n.2291C=
19	g.35284807C>G	CA405300581	HAMP	c.109C>G (p.Leu37Val) n.2291C>G
19	g.35284807C>T	CA507041010	HAMP	c.109C>T (p.Leu37=) n.2291C>T	dbSNP gnomAD v2 gnomAD v4
19	g.35284808T>A	CA405300586	HAMP	c.110T>A (p.Leu37Gln) n.2292T>A	dbSNP gnomAD v3 gnomAD v4
19	g.35284808T>C	CA405300584	HAMP	c.110T>C (p.Leu37Pro) n.2292T>C	dbSNP gnomAD v2 gnomAD v4
19	g.35284808T>G	CA405300585	HAMP	c.110T>G (p.Leu37Arg) n.2292T>G
19	g.35284808T=	CA2333586018	HAMP	c.110T= (p.Leu37=) n.2292T=
19	g.35284809G>A	CA507041026	HAMP	c.111G>A (p.Leu37=) n.2293G>A	dbSNP gnomAD v2 gnomAD v4
19	g.35284809G>C	CA507041029	HAMP	c.111G>C (p.Leu37=) n.2293G>C
19	g.35284809G=	CA2333586019	HAMP	c.111G= (p.Leu37=) n.2293G=
19	g.35284809G>T	CA507041032	HAMP	c.111G>T (p.Leu37=) n.2293G>T
19	g.35284810C>A	CA405300587	HAMP	c.112C>A (p.Gln38Lys) n.2294C>A
19	g.35284810C>G	CA405300588	HAMP	c.112C>G (p.Gln38Glu) n.2294C>G
19	g.35284810C>T	CA405300590	HAMP	c.112C>T (p.Gln38Ter) n.2294C>T
19	g.35284811A>C	CA405300593	HAMP	c.113A>C (p.Gln38Pro) n.2295A>C
19	g.35284811A>G	CA405300598	HAMP	c.113A>G (p.Gln38Arg) n.2295A>G
19	g.35284811A>T	CA405300601	HAMP	c.113A>T (p.Gln38Leu) n.2295A>T
19	g.35284812del	CA2695228583	HAMP	c.114del (p.Gln38HisfsTer?) n.2296del
19	g.35284812A=	CA2333586020	HAMP	c.114A= (p.Gln38=) n.2296A=
19	g.35284812A>C	CA405300606	HAMP	c.114A>C (p.Gln38His) n.2296A>C
19	g.35284812A>G	CA507041061	HAMP	c.114A>G (p.Gln38=) n.2296A>G	ClinVar dbSNP
19	g.35284812A>T	CA405300610	HAMP	c.114A>T (p.Gln38His) n.2296A>T
19	g.35284813C>A	CA405300614	HAMP	c.115C>A (p.Pro39Thr) n.2297C>A
19	g.35284813C=	CA2333586021	HAMP	c.115C= (p.Pro39=) n.2297C=
19	g.35284813C>G	CA405300617	HAMP	c.115C>G (p.Pro39Ala) n.2297C>G
19	g.35284813C>T	CA9375793	HAMP	c.115C>T (p.Pro39Ser) n.2297C>T	dbSNP ExAC gnomAD v2 gnomAD v4
19	g.35284814C>A	CA405300626	HAMP	c.116C>A (p.Pro39His) n.2298C>A	gnomAD v4
19	g.35284814C>G	CA405300628	HAMP	c.116C>G (p.Pro39Arg) n.2298C>G
19	g.35284814C>T	CA405300624	HAMP	c.116C>T (p.Pro39Leu) n.2298C>T	gnomAD v4
19	g.35284815C>A	CA507041078	HAMP	c.117C>A (p.Pro39=) n.2299C>A
19	g.35284815C=	CA2333586022	HAMP	c.117C= (p.Pro39=) n.2299C=
19	g.35284815C>G	CA507041081	HAMP	c.117C>G (p.Pro39=) n.2299C>G
19	g.35284815C>T	CA9375794	HAMP	c.117C>T (p.Pro39=) n.2299C>T	dbSNP ExAC gnomAD v2 gnomAD v4
19	g.35284816C>A	CA405300640	HAMP	c.118C>A (p.Gln40Lys) n.2300C>A
19	g.35284816C>G	CA405300649	HAMP	c.118C>G (p.Gln40Glu) n.2300C>G
19	g.35284816C>T	CA405300655	HAMP	c.118C>T (p.Gln40Ter) n.2300C>T
19	g.35284817A=	CA2333586023	HAMP	c.119A= (p.Gln40=) n.2301A=

Number of alleles fetched