Variant #0000000153 (NC_000011.9:g.5275637T>C, HBG2(NM_000184.2):c.200A>G)
Chromosome |
11 |
Allele |
Parent #1 |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5275637T>C |
Reference |
Zeng et al;dbSNP |
DB-ID |
HBG2_000017 |
Frequency |
- |
Variant remarks |
Hb F-Shanghai |
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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