Variant #0000000293 (NC_000011.9:g.5248329T>G, HBB(NM_000518.4):c.-78A>C)
| Individual ID |
00000224, 00000429, 00000686, 00001074, 00001609 |
| Chromosome |
11 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5248329T>G |
| Reference |
(OMIM 0380);dbSNP;Poncz M et al.; |
| DB-ID |
HBB_000022 |
| Frequency |
- |
| Variant remarks |
-28 (A->C) beta+ |
| 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
Screenings
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