Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.5225488A>G | CA213889 | HBB | c.*110T>C (n.*110T>C) c.*370T>C (n.*370T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.5225488A>T | CA217112088 | HBB | c.*110T>A (n.*110T>A) c.*370T>A (n.*370T>A) | ClinVar dbSNP gnomAD v4 |
11 | g.5225488A= | CA1949563725 | HBB | c.*110T= (n.*110T=) c.*370T= (n.*370T=) | dbSNP |