Variant #0000000318 (NC_000011.9:g.5246909_5268823del, HBB(NM_000518.4):c.-20572_363del)
Chromosome |
11 |
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.5246909_5268823del |
Reference |
Shang et al |
DB-ID |
HBD_000027 See all 2 reported entries |
Frequency |
- |
Variant remarks |
21.9k del |
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
|
|