Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.173128G>A | CA276414541 | HBA2 | c.99G>A (p.Met33Ile) c.3G>A (p.Met1Ile) n.235G>A n.68G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.173128G= | CA2200880625 | HBA2 | c.99G= (p.Met33=) c.3G= (p.Met1=) n.235G= n.68G= | dbSNP |