Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5225614G>ACA037606HBBc.428C>T (p.Ala143Val)
c.*244C>T (n.*244C>T)
ClinVar dbSNP
11g.5225614G>TCA125074HBBc.428C>A (p.Ala143Asp)
c.*244C>A (n.*244C>A)
ClinVar dbSNP
11g.5225614G=CA1949564243HBBc.428C= (p.Ala143=)
c.*244C= (n.*244C=)
dbSNP

Number of alleles fetched