Linked Data
dbSNP Id:
rs1033025898
gnomAD v2:
2-10587715-T-C
gnomAD v3:
2-10447589-T-C
gnomAD v4:
2-10447589-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.10447589T>C , CM000664.2:g.10447589T>C | GRCh38 |
| NC_000002.11:g.10587715T>C , CM000664.1:g.10587715T>C | GRCh37 |
| NC_000002.10:g.10505166T>C | NCBI36 |
| NG_012105.1:g.5739A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000443218.2:c.-128+39A>G | ENSP00000390691.2:n.-128+39A>G | |
| ENST00000446285.6:c.-128+532A>G | ENSP00000514632.1:n.-128+532A>G | |
| ENST00000699835.1:c.-533A>G | ENSP00000514633.1:n.-533A>G | |
| ENST00000699836.1:c.-18+532A>G | ENSP00000514634.1:n.-18+532A>G | |
| ENST00000234111.9:c.-128+532A>G MANE Select | ENSP00000234111.4:n.-128+532A>G | |
| ENST00000234111.8:c.-128+532A>G | ENSP00000234111.4:n.-128+532A>G | |
| ENST00000405333.5:c.-243A>G | ENSP00000385333.1:n.-243A>G | |
| ENST00000443218.1:c.-128+39A>G | ENSP00000390691.1:n.-128+39A>G | |
| ENST00000446285.5:n.189+532A>G | ||
| NM_001287188.1:c.-415+532A>G | NP_001274117.1:n.-415+532A>G | |
| NM_001287189.1:c.-243A>G | NP_001274118.1:n.-243A>G | |
| NM_001287190.1:c.-128+39A>G | NP_001274119.1:n.-128+39A>G | |
| NM_002539.2:c.-128+532A>G | NP_002530.1:n.-128+532A>G | |
| NM_002539.3:c.-128+532A>G MANE Select | NP_002530.1:n.-128+532A>G | |
| NM_001287188.2:c.-415+532A>G | NP_001274117.1:n.-415+532A>G | |
| NM_001287189.2:c.-243A>G | NP_001274118.1:n.-243A>G | |
| NM_001287190.2:c.-128+39A>G | NP_001274119.1:n.-128+39A>G |