Variant #0000000997 (NC_000016.9:g.222951G>T, HBA2(NM_000517.4):c.40G>T)
Individual ID |
00001020 |
Chromosome |
16 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.222951G>T |
Reference |
Xiong et al |
DB-ID |
HBA2_000023 |
Frequency |
- |
Variant remarks |
Hb Binyang |
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
Screenings
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