Variant #0000000307 (NC_000011.9:g.5248330T>C, HBB(NM_000518.4):c.-79A>G)
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.5248330T>C |
Reference |
(OMIM 0379);dbSNP;Chen et al. |
DB-ID |
HBB_000005 See all 2 reported entries |
Frequency |
- |
Variant remarks |
-29 (A->G) |
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
|