| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.5225606A>T | CA217112211 | HBB | c.436T>A (p.Tyr146Asn) c.*252T>A (n.*252T>A) | ClinVar dbSNP |
| 11 | g.5225606A>G | CA124752 | HBB | c.436T>C (p.Tyr146His) c.*252T>C (n.*252T>C) | ClinVar dbSNP |
| 11 | g.5225606A>C | CA217112207 | HBB | c.436T>G (p.Tyr146Asp) c.*252T>G (n.*252T>G) | dbSNP |