Variant #0000000117 (NC_000011.9:g.5276169G>A, HBG2(NM_000184.2):c.-211C>T)
Chromosome |
11 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5276169G>A |
Reference |
GenBank;dbSNP |
DB-ID |
HBG2_000008 See all 3 reported entries |
Frequency |
- |
Variant remarks |
- |
ClassClinical |
uncertain significance |
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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