Variant #0000001002 (NC_000016.9:g.222968C>T, HBA2(NM_000517.4):c.57C>T)
| Chromosome |
16 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.222968C>T |
| Reference |
Lin et al |
| DB-ID |
HBA2_000031 |
| Frequency |
- |
| Variant remarks |
Hb Debao |
| ClassClinical |
Pathogenic |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Qi Ming |
| Database submission license |
No license selected |
| Created by |
Qi Ming |

Variant on transcripts
|
|