Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
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=
19	g.35284817A>C	CA405300658	HAMP	c.119A>C (p.Gln40Pro) n.2301A>C	dbSNP
19	g.35284817A>G	CA405300659	HAMP	c.119A>G (p.Gln40Arg) n.2301A>G	dbSNP gnomAD v4
19	g.35284817A>T	CA405300660	HAMP	c.119A>T (p.Gln40Leu) n.2301A>T
19	g.35284818G>A	CA507041096	HAMP	c.120G>A (p.Gln40=) n.2302G>A
19	g.35284818G>C	CA405300662	HAMP	c.120G>C (p.Gln40His) n.2302G>C
19	g.35284818G>T	CA405300664	HAMP	c.120G>T (p.Gln40His) n.2302G>T
19	g.35284819G>A	CA405300667	HAMP	c.121G>A (p.Asp41Asn) n.2303G>A	dbSNP gnomAD v4
19	g.35284819G>C	CA405300677	HAMP	c.121G>C (p.Asp41His) n.2303G>C
19	g.35284819G=	CA2333586024	HAMP	c.121G= (p.Asp41=) n.2303G=
19	g.35284819G>T	CA405300690	HAMP	c.121G>T (p.Asp41Tyr) n.2303G>T
19	g.35284820A>C	CA405300696	HAMP	c.122A>C (p.Asp41Ala) n.2304A>C
19	g.35284820A>G	CA405300699	HAMP	c.122A>G (p.Asp41Gly) n.2304A>G
19	g.35284820A>T	CA405300694	HAMP	c.122A>T (p.Asp41Val) n.2304A>T
19	g.35284821C>A	CA405300702	HAMP	c.123C>A (p.Asp41Glu) n.2305C>A
19	g.35284821C>G	CA405300703	HAMP	c.123C>G (p.Asp41Glu) n.2305C>G
19	g.35284821C>T	CA507041122	HAMP	c.123C>T (p.Asp41=) n.2305C>T
19	g.35284821_35284823delinsCAG	CA2333586025	HAMP	c.123_125delinsCAG (p.Asp41=) n.2305_2307delinsCAG
19	g.35284822A>C	CA507041126	HAMP	c.124A>C (p.Arg42=) n.2306A>C
19	g.35284822A>G	CA405300708	HAMP	c.124A>G (p.Arg42Gly) n.2306A>G
19	g.35284822A>T	CA405300712	HAMP	c.124A>T (p.Arg42Ter) n.2306A>T

Number of alleles fetched