| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.173563C>A | CA276415481 | HBA2 | c.392C>A (p.Ala131Asp) c.296C>A (p.Ala99Asp) n.528C>A | dbSNP |
| 16 | g.173563C>T | CA393994617 | HBA2 | c.392C>T (p.Ala131Val) c.296C>T (p.Ala99Val) n.528C>T | dbSNP |
| 16 | g.173563C= | CA2200880957 | HBA2 | c.392C= (p.Ala131=) c.296C= (p.Ala99=) n.528C= | dbSNP |