Linked Data
dbSNP Id:
rs1160110321
gnomAD v2:
6-32009025-T-C
gnomAD v3:
6-32041248-T-C
gnomAD v4:
6-32041248-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32041248T>C , CM000668.2:g.32041248T>C | GRCh38 |
| NC_000006.11:g.32009025T>C , CM000668.1:g.32009025T>C | GRCh37 |
| NC_000006.10:g.32117004T>C | NCBI36 |
| NG_007941.2:g.7941T>C | |
| NG_008337.2:g.73127A>G | |
| NG_007941.3:g.7944T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644719.2:c.*114T>C (CYP21A2) MANE Select | ENSP00000496625.1:n.*114T>C | |
| ENST00000644971.2:c.*101A>G (TNXB) MANE Select | ENSP00000496448.1:n.*101A>G | |
| ENST00000647633.1:c.*101A>G (TNXB) | ENSP00000497649.1:n.*101A>G | |
| ENST00000375244.7:c.*101A>G (TNXB) | ENSP00000364393.3:n.*101A>G | |
| ENST00000418967.6:c.*114T>C (CYP21A2) | ENSP00000408860.2:n.*114T>C | |
| ENST00000435122.3:c.*114T>C (CYP21A2) | ENSP00000415043.2:n.*114T>C | |
| ENST00000451343.4:c.*101A>G (TNXB) | ENSP00000407685.1:n.*101A>G | |
| ENST00000479074.5:n.1743T>C (CYP21A2) | ||
| ENST00000479730.5:n.1718T>C (CYP21A2) | ||
| ENST00000486063.5:n.1581T>C (CYP21A2) | ||
| ENST00000490077.5:n.2663A>G (TNXB) | ||
| ENST00000611016.2:c.5990A>G (TNXB) | ENSP00000483409.1:n.5990A>G | |
| NM_000500.7:c.*114T>C (CYP21A2) | NP_000491.4:n.*114T>C | |
| NM_001128590.3:c.*114T>C (CYP21A2) | NP_001122062.3:n.*114T>C | |
| NM_019105.6:c.*101A>G (TNXB) | NP_061978.6:n.*101A>G | |
| NM_032470.3:c.*101A>G (TNXB) | NP_115859.2:n.*101A>G | |
| XM_011514314.1:c.*114T>C (CYP21A2) | XP_011512616.1:n.*114T>C | |
| NM_000500.9:c.*114T>C (CYP21A2) MANE Select | NP_000491.4:n.*114T>C | |
| NM_001365276.1:c.*101A>G (TNXB) | NP_001352205.1:n.*101A>G | |
| NM_019105.7:c.*101A>G (TNXB) | NP_061978.6:n.*101A>G | |
| NM_001365276.2:c.*101A>G (TNXB) MANE Select | NP_001352205.1:n.*101A>G | |
| NM_001368143.1:c.*114T>C (CYP21A2) | NP_001355072.1:n.*114T>C | |
| NM_001368144.1:c.*114T>C (CYP21A2) | NP_001355073.1:n.*114T>C | |
| NM_019105.8:c.*101A>G (TNXB) | NP_061978.6:n.*101A>G | |
| NM_001128590.4:c.*114T>C (CYP21A2) | NP_001122062.3:n.*114T>C | |
| NM_001368143.2:c.*114T>C (CYP21A2) | NP_001355072.1:n.*114T>C | |
| NM_001368144.2:c.*114T>C (CYP21A2) | NP_001355073.1:n.*114T>C | |
| NM_032470.4:c.*101A>G (TNXB) | NP_115859.2:n.*101A>G |