Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.177392T>C | CA276417285 | HBA1 | c.410T>C (p.Leu137Pro) c.314T>C (p.Leu105Pro) n.546T>C | dbSNP |
16 | g.177392T>G | CA215116 | HBA1 | c.410T>G (p.Leu137Arg) c.314T>G (p.Leu105Arg) n.546T>G | ClinVar dbSNP |
16 | g.177392T= | CA2200883316 | HBA1 | c.410T= (p.Leu137=) c.314T= (p.Leu105=) n.546T= | dbSNP |