Variant #0000000378 (NC_000011.9:g.5248173C>T, HBB(NM_000518.4):c.79G>A)
| Chromosome |
11 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5248173C>T |
| Reference |
(OMIM 0071);dbSNP;Flatz G et al.;Indrak K et al.;Kazazian HH Jr et al.; |
| DB-ID |
HBB_000051 See all 2 reported entries |
| Frequency |
- |
| Variant remarks |
Hb E |
| 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
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