Variant #0000603974 (NC_000011.9:g.5248211_5248236del, HBB(NM_000518.4):c.20_45del)

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.5248211_5248236del
DNA change (hg38) g.5226981_5227006del
Published as CD 6-14 (-26 bp) (26 bp deletion), 20_45del26bp
ISCN -
DB-ID HBB_001791 See all 2 reported entries
Variant remarks β-thalassaemia, Haemolytic anaemia, Ineffective erythropoiesis
Reference IthaNet-2184
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner IthaNet - Petros Kountouris
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 +/. - c.20_45del - r.(?) p.(Glu7Valfs*8)