Variant #0000001004 (NC_000016.9:g.223151delG, HBA2(NM_000517.4):c.123delG)
Chromosome |
16 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Deletion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.223151delG |
Reference |
So et al |
DB-ID |
HBA2_000032 |
Frequency |
- |
Variant remarks |
Codon41(-G) |
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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