Variant #0000000965 (NC_000016.9:g.123895_245125dup, HBA2(NM_000517.4):c.-99017_*21526dup)

Chromosome 16
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.123895_245125dup
Reference Shang et al
DB-ID HBA2_000006 See all 2 reported entries
Frequency -
Variant remarks αααα121.2
ClassClinical Uncertain significance
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBA2 NM_000517.4 ./. 01-03 c.-99017_*21526dup r.0? p.0?