Variant #0000000395 (NC_000011.9:g.5248155C>G, HBB(NM_000518.4):c.92+5G>C)
Chromosome |
11 |
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.5248155C>G |
Reference |
(OMIM 0357);dbSNP;Kulozik AE et al.;Treisman R et al.;Divoky V et al.;Kazazian HH Jr et al.; |
DB-ID |
HBB_000061 |
Frequency |
- |
Variant remarks |
IVS-I-5 (G->C) beta+ (severe) |
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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