Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.177096A>C | CA276416985 | HBA1 | c.263A>C (p.His88Pro) c.167A>C (p.His56Pro) n.399A>C n.232A>C | dbSNP |
16 | g.177096A>G | CA125761 | HBA1 | c.263A>G (p.His88Arg) c.167A>G (p.His56Arg) n.399A>G n.232A>G | ClinVar dbSNP |
16 | g.177096A= | CA2200883096 | HBA1 | c.263A= (p.His88=) c.167A= (p.His56=) n.399A= n.232A= | dbSNP |