Variant #0000016124 (NC_000011.9:g.5247862_5247863delinsAT, HBB(NM_000518.4):c.259_260delinsAT)
| Chromosome |
11 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Insertion/Deletion |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5247862_5247863delinsAT |
| Reference |
Shang X,et al.(2017) |
| DB-ID |
HBB_000009 |
| Frequency |
- |
| Variant remarks |
- |
| ClassClinical |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Qianqian Zhang |
| Database submission license |
No license selected |
| Created by |
Qianqian Zhang |

Variant on transcripts
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