Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
6	g.49612504C>A	CA364398543	RHAG	c.838G>T (p.Gly280Ter) n.528G>T
6	g.49612504C=	CA1627469181	RHAG	c.838G= (p.Gly280=) n.528G=
6	g.49612504C>G	CA364398542	RHAG	c.838G>C (p.Gly280Arg) n.528G>C
6	g.49612504C>T	CA357864	RHAG	c.838G>A (p.Gly280Arg) n.528G>A	dbSNP gnomAD v4
6	g.[49612504C>T;49612534C>T]	CA357865	RHAG	c.[808G>A;838G>A] (p.[Val270Ile;Gly280Arg]) n.[498G>A;528G>A]	ClinVar
6	g.49612505T>A	CA450401591	RHAG	c.837A>T (p.Gly279=) n.527A>T	dbSNP gnomAD v2 gnomAD v4
6	g.49612505T>C	CA450401592	RHAG	c.837A>G (p.Gly279=) n.527A>G	gnomAD v4
6	g.49612505T>G	CA450401593	RHAG	c.837A>C (p.Gly279=) n.527A>C
6	g.49612505T=	CA1627469187	RHAG	c.837A= (p.Gly279=) n.527A=
6	g.49612506C>A	CA364398544	RHAG	c.836G>T (p.Gly279Val) n.526G>T
6	g.49612506C=	CA1627469194	RHAG	c.836G= (p.Gly279=) n.526G=
6	g.49612506C>G	CA364398545	RHAG	c.836G>C (p.Gly279Ala) n.526G>C	dbSNP
6	g.49612506C>T	CA122828	RHAG	c.836G>A (p.Gly279Glu) n.526G>A	ClinVar dbSNP gnomAD v2 gnomAD v4
6	g.49612507C>A	CA364398546	RHAG	c.835G>T (p.Gly279Ter) n.525G>T	COSMIC
6	g.49612507C>G	CA364398547	RHAG	c.835G>C (p.Gly279Arg) n.525G>C
6	g.49612507C>T	CA364398548	RHAG	c.835G>A (p.Gly279Arg) n.525G>A
6	g.49612508A=	CA1627469198	RHAG	c.834T= (p.Ala278=) n.524T=
6	g.49612508A>C	CA3847802	RHAG	c.834T>G (p.Ala278=) n.524T>G	dbSNP ExAC gnomAD v2
6	g.49612508A>G	CA450401595	RHAG	c.834T>C (p.Ala278=) n.524T>C	gnomAD v4
6	g.49612508A>T	CA450401596	RHAG	c.834T>A (p.Ala278=) n.524T>A
6	g.49612509G>A	CA364398550	RHAG	c.833C>T (p.Ala278Val) n.523C>T
6	g.49612509G>C	CA364398549	RHAG	c.833C>G (p.Ala278Gly) n.523C>G
6	g.49612509G>T	CA364398551	RHAG	c.833C>A (p.Ala278Asp) n.523C>A
6	g.49612510C>A	CA364398552	RHAG	c.832G>T (p.Ala278Ser) n.522G>T	dbSNP gnomAD v2 gnomAD v4
6	g.49612510C=	CA1627469206	RHAG	c.832G= (p.Ala278=) n.522G=
6	g.49612510C>G	CA364398554	RHAG	c.832G>C (p.Ala278Pro) n.522G>C
6	g.49612510C>T	CA364398553	RHAG	c.832G>A (p.Ala278Thr) n.522G>A
6	g.49612511A>C	CA450401599	RHAG	c.831T>G (p.Leu277=) n.521T>G
6	g.49612511A>G	CA450401600	RHAG	c.831T>C (p.Leu277=) n.521T>C	gnomAD v4
6	g.49612511A>T	CA450401598	RHAG	c.831T>A (p.Leu277=) n.521T>A
6	g.49612512A>C	CA364398555	RHAG	c.830T>G (p.Leu277Arg) n.520T>G
6	g.49612512A>G	CA364398556	RHAG	c.830T>C (p.Leu277Pro) n.520T>C
6	g.49612512A>T	CA364398557	RHAG	c.830T>A (p.Leu277His) n.520T>A
6	g.49612513G>A	CA364398558	RHAG	c.829C>T (p.Leu277Phe) n.519C>T
6	g.49612513G>C	CA364398559	RHAG	c.829C>G (p.Leu277Val) n.519C>G	gnomAD v4
6	g.49612513G>T	CA364398560	RHAG	c.829C>A (p.Leu277Ile) n.519C>A
6	g.49612514G>A	CA450401606	RHAG	c.828C>T (p.Thr276=) n.518C>T
6	g.49612514G>C	CA450401605	RHAG	c.828C>G (p.Thr276=) n.518C>G
6	g.49612514G>T	CA450401604	RHAG	c.828C>A (p.Thr276=) n.518C>A
6	g.49612515G>A	CA364398561	RHAG	c.827C>T (p.Thr276Ile) n.517C>T	dbSNP gnomAD v2 gnomAD v4
6	g.49612515G>C	CA364398562	RHAG	c.827C>G (p.Thr276Ser) n.517C>G	ClinVar
6	g.49612515G=	CA1627469209	RHAG	c.827C= (p.Thr276=) n.517C=
6	g.49612515G>T	CA364398563	RHAG	c.827C>A (p.Thr276Asn) n.517C>A
6	g.49612516T>A	CA364398564	RHAG	c.826A>T (p.Thr276Ser) n.516A>T	gnomAD v4
6	g.49612516T>C	CA364398565	RHAG	c.826A>G (p.Thr276Ala) n.516A>G
6	g.49612516T>G	CA364398566	RHAG	c.826A>C (p.Thr276Pro) n.516A>C
6	g.49612517G>A	CA450401610	RHAG	c.825C>T (p.Ala275=) n.515C>T
6	g.49612517G>C	CA450401608	RHAG	c.825C>G (p.Ala275=) n.515C>G
6	g.49612517G>T	CA450401609	RHAG	c.825C>A (p.Ala275=) n.515C>A
6	g.49612518G>A	CA138843690	RHAG	c.824C>T (p.Ala275Val) n.514C>T	dbSNP

Number of alleles fetched