Variant #0000603923 (NC_000011.9:g.5222877_5250289del, NM_000518.4:c.-2038_*23951del (HBB))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5222877_5250289del |
| DNA change (hg38) |
g.5201647_5229059del |
| Published as |
Vietnamese, SE Asian (HPFH-7, SEA-HPFH), NC_000011.10:g.5201647-5229059del27412bp |
| ISCN |
- |
| DB-ID |
HBB_004012 |
| Variant remarks |
HPFH, Hb F levels |
| Reference |
IthaNet-1505 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
IthaNet - Petros Kountouris |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2019-11-08 15:46:08 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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