Variant #0000000980 (NC_000016.9:g.220158_226502del, HBA2(NM_000517.4):c.-2754_*2903del)
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.220158_226502del |
Reference |
Wang et al |
DB-ID |
HBA2_000010 |
Frequency |
- |
Variant remarks |
-a6.3 |
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
|
|