Variant #0000001004 (NC_000016.9:g.223151delG, HBA2(NM_000517.4):c.123delG)
| 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.223151delG |
| Reference |
So et al |
| DB-ID |
HBA2_000032 |
| Frequency |
- |
| Variant remarks |
Codon41(-G) |
| 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
|
|