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 |

Variant on transcripts
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