Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.173551A>G | CA276415454 | HBA2 | c.380A>G (p.Asp127Gly) c.284A>G (p.Asp95Gly) n.516A>G | ClinVar dbSNP |
16 | g.173551A>T | CA276415455 | HBA2 | c.380A>T (p.Asp127Val) c.284A>T (p.Asp95Val) n.516A>T | dbSNP |
16 | g.173551A= | CA2200880950 | HBA2 | c.380A= (p.Asp127=) c.284A= (p.Asp95=) n.516A= | dbSNP |