Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5226600G>TCA125523HBBc.292C>A (p.His98Asn)
n.224C>A
n.343C>A
c.*108C>A (n.*108C>A)
 ClinVar dbSNP
11g.5226600G>ACA125040HBBc.292C>T (p.His98Tyr)
n.224C>T
n.343C>T
c.*108C>T (n.*108C>T)
 ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched