Variant #0000000303 (NC_000011.9:g.5248259_5248262delGTTT, HBB(NM_000518.4):c.-11_-8delAAAC)

Chromosome 11
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.5248259_5248262delGTTT
Reference Huang et al;dbSNP
DB-ID HBB_000029
Frequency -
Variant remarks Cap +43/+40 (-AAAC)
ClassClinical Pathogenic
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBB NM_000518.4 ./. 01 c.-11_-8delAAAC r.(=) p.(=)