Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5226576C>GCA346836HBBc.315+1G>C (p.=)
n.247+1G>C
n.367G>C
c.*131+1G>C (p.=)
ClinVar dbSNP
11g.5226576C>TCA125305HBBc.315+1G>A (p.=)
n.247+1G>A
n.367G>A
c.*131+1G>A (p.=)
ClinVar dbSNP ExAC gnomAD
11g.5226576C>ACA217113399HBBc.315+1G>T (p.=)
n.247+1G>T
n.367G>T
c.*131+1G>T (p.=)
ClinVar dbSNP

Number of alleles fetched