| 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 |
