Variant #0000000270 (NC_000011.9:g.5254286T>C, HBD(NM_000519.3):c.352A>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.5254286T>C |
Reference |
dbSNP;Qin et al |
DB-ID |
HBD_000042 |
Frequency |
- |
Variant remarks |
HbA2 liangcheng |
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
|
|