| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.5226600G>T | CA125523 | HBB | c.292C>A (p.His98Asn) n.224C>A n.343C>A c.*108C>A (n.*108C>A) | ClinVar dbSNP |
| 11 | g.5226600G>A | CA125040 | HBB | c.292C>T (p.His98Tyr) n.224C>T n.343C>T c.*108C>T (n.*108C>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.5226600G= | CA1949567548 | HBB | c.292C= (p.His98=) n.224C= n.343C= c.*108C= (n.*108C=) | dbSNP |