Variant #0000001065 (NC_000016.9:g.227251_227258delinsG, HBA1(NM_000558.3):c.301-31_301-24delinsG)

Chromosome 16
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.227251_227258delinsG
Reference -
DB-ID HBA1_000001
Frequency -
Variant remarks Case report of two reorganize forms of HBA1 and HBA2 genes
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     
HBA1 NM_000558.3 ./. 03 c.301-31_301-24delinsG r.(=) p.(=)