| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.5226981G>T | CA124955 | HBB | c.41C>A (p.Ala14Asp) n.92C>A | ClinVar dbSNP COSMIC |
| 11 | g.5226981G>C | CA379274904 | HBB | c.41C>G (p.Ala14Gly) n.92C>G | dbSNP |
| 11 | g.5226981G>A | CA379274902 | HBB | c.41C>T (p.Ala14Val) n.92C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.5226981G= | CA1949570780 | HBB | c.41C= (p.Ala14=) n.92C= | dbSNP |