| Variant #0000603376 (NC_000011.9:g.5246963G>C, NC_000011.9(NM_000518.4):c.316-7C>G (HBB))
        
          | Chromosome | 11 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.5246963G>C |  
          | DNA change (hg38) | g.5225733G>C |  
          | Published as | IVS II-844 (C>G) |  
          | ISCN | - |  
          | DB-ID | HBB_001211 See all 2 reported entries |  
          | Variant remarks | β-thalassaemia, Haemolytic anaemia, Ineffective erythropoiesis |  
          | Reference | IthaNet-220 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | IthaNet - Petros Kountouris |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2019-11-08 15:46:08 +01:00 (CET) |  
          | Date last edited | 2020-06-29 17:30:45 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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