Variant #0000000998 (NC_000016.9:g.222957G>A, HBA2(NM_000517.4):c.46G>A)

Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.222957G>A
Reference Yao et al
DB-ID HBA2_000022
Frequency -
Variant remarks Codon16(G>A)
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     
HBA2 NM_000517.4 ./. 01 c.46G>A r.(?) p.(Gly16Ser)