Variant #0000000371 (NC_000011.9:g.5248184T>G, HBB(NM_000518.4):c.68A>C)
Chromosome |
11 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5248184T>G |
Reference |
(OMIM 0081);dbSNP;Li J et al.;el-Hashemite N et al.;Dincol G et al.;Blackwell RQ et al.; |
DB-ID |
HBB_000049 |
Frequency |
- |
Variant remarks |
Hb G-Coushatta |
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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