Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.173295C>G | CA276415009 | HBA2 | c.266C>G (p.Ala89Gly) c.170C>G (p.Ala57Gly) n.402C>G n.235C>G | ClinVar dbSNP |
16 | g.173295C>T | CA125554 | HBA2 | c.266C>T (p.Ala89Val) c.170C>T (p.Ala57Val) n.402C>T n.235C>T | ClinVar dbSNP |
16 | g.173295C>A | CA276415006 | HBA2 | c.266C>A (p.Ala89Glu) c.170C>A (p.Ala57Glu) n.402C>A n.235C>A | dbSNP |