Variant #0000000361 (NC_000011.9:g.5248206_5248207insC, HBB(NM_000518.4):c.45_46insG)
Chromosome |
11 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Insertion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5248206_5248207insC |
Reference |
Xiong et al |
DB-ID |
HBB_000045 |
Frequency |
- |
Variant remarks |
Codons 14/15 (+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
|
|