| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.5226615G>C | CA124927 | HBB | c.277C>G (p.His93Asp) n.209C>G n.328C>G c.*93C>G (n.*93C>G) | ClinVar dbSNP |
| 11 | g.5226615G>A | CA125009 | HBB | c.277C>T (p.His93Tyr) n.209C>T n.328C>T c.*93C>T (n.*93C>T) | ClinVar dbSNP |
| 11 | g.5226615G>T | CA125357 | HBB | c.277C>A (p.His93Asn) n.209C>A n.328C>A c.*93C>A (n.*93C>A) | ClinVar dbSNP |