Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.5225611T>A | CA217112264 | HBB | c.431A>T (p.His144Leu) c.*247A>T (n.*247A>T) | dbSNP |
11 | g.5225611T>C | CA124714 | HBB | c.431A>G (p.His144Arg) c.*247A>G (n.*247A>G) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.5225611T>G | CA125192 | HBB | c.431A>C (p.His144Pro) c.*247A>C (n.*247A>C) | ClinVar dbSNP |