Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5227019C>TCA125383HBBc.3G>A (p.Met1Ile)
n.54G>A
ClinVar dbSNP
11g.5227019C>GCA217115643HBBc.3G>C (p.Met1Ile)
n.54G>C
ClinVar dbSNP
11g.5227019C>ACA217115639HBBc.3G>T (p.Met1Ile)
n.54G>T
ClinVar dbSNP

Number of alleles fetched