Variant #0000000151 (NC_000011.9:g.5217204_5285011dup, HBG2(NM_000184.2):c.-9053_*57303dup)

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Duplication
DNA change (genomic) (Relative to hg19 / GRCh37) g.5217204_5285011dup
Reference Shang et al
DB-ID HBD_000025 See all 4 reported entries
Frequency -
Variant remarks β67.8k dup
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     
HBG2 NM_000184.2 ./. 01-03 c.-9053_*57303dup r.0? p.0?