Variant #0000000967 (NC_000016.9:g.194214_238840del, HBA2(NM_000517.4):c.-28698_*15241del)
| Chromosome |
16 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Deletion |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.194214_238840del |
| Reference |
Wang et al |
| DB-ID |
HBA1_000003 See all 2 reported entries |
| Frequency |
- |
| Variant remarks |
- -44.6 |
| 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
|
|