Variant #0000000235 (NC_000011.9:g.5270026_5274949del, HBG1(NM_000559.2):c.-3915_316-309del)

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.5270026_5274949del
Reference Cai et al
DB-ID HBG1_000012
Frequency -
Variant remarks Uncertain significant
ClassClinical Uncertain significance
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBG1 NM_000559.2 ./. 01-03 c.-3915_316-309del r.? p.?