Variant #0000000111 (NC_000011.9:g.5274452_5274453insT, HBG2(NM_000184.2):c.*54_*55insA)
Individual ID |
00000017, 00000049, 00000104, 00000155, 00000362, 00000390, 00000636, 00000638, 00000738, 00000805, 00001086, 00001138, 00001564, 00001749, 00001755, 00002003, 00002050 |
Chromosome |
11 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Type |
Insertion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5274452_5274453insT |
Reference |
GenBank;dbSNP |
DB-ID |
HBG2_000002 |
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
Screenings
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