Variant #0000001131 (NC_000016.9:g.97115_175257del)
Individual ID |
00001972 |
Chromosome |
16 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Type |
Deletion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.97115_175257del |
Reference |
Shang et al |
DB-ID |
HBA1_000002 See all 2 reported entries |
Frequency |
- |
Variant remarks |
-a78 |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
Screenings
|
|