Variant #0000016124 (NC_000011.9:g.5247862_5247863delinsAT, HBB(NM_000518.4):c.259_260delinsAT)

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Insertion/Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.5247862_5247863delinsAT
Reference Shang X,et al.(2017)
DB-ID HBB_000009
Frequency -
Variant remarks -
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qianqian Zhang
Database submission license No license selected
Created by Qianqian Zhang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBB NM_000518.4 ./. 2 c.259_260delinsAT r.(?) p.(Ala87Ile)