rs4073054
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Locations
| Assembly | Sequence | Position | Alleles | Source |
|---|---|---|---|---|
| GRCh38 | NC_000001.11(opens in new window) | 161230697 |
| dbSnp |
| GRCh37 | NC_000001.10(opens in new window) | 161200487 |
| dbSnp |
| NG_029113.1(opens in new window) | 12514 |
| dbSnp |
Variant Frequencies
Identifiers
PharmGKB ID
Aliases
- rs17393733 (retired)
- rs386590491 (retired)
- rs56504295 (retired)
- rs57597870 (retired)
- NC_000001.10:g.161200487C>A
- NC_000001.11:g.161230697C>A
- NG_029113.1:g.12514G>T
- NM_001077469.2:c.932+116G>T
- NM_001077470.2:c.713+116G>T
- NM_001077471.2:c.800+116G>T
- NM_001077472.2:c.845+116G>T
- NM_001077473.2:c.857+116G>T
- NM_001077474.2:c.800+116G>T
- NM_001077475.2:c.713+116G>T
- NM_001077476.2:c.845+116G>T
- NM_001077477.2:c.830+116G>T
- NM_001077478.2:c.929+116G>T
- NM_001077479.2:c.830+116G>T
- NM_001077480.2:c.929+116G>T
- NM_001077481.2:c.815+116G>T
- NM_001077482.2:c.944+116G>T
- NM_001286373.1:c.*1602C>A
- NM_001286374.1:c.*1602C>A
- NM_005122.4:c.917+116G>T
- NM_032174.5:c.*1602C>A
- XM_005245536.1:c.*1602C>A
- XM_005245537.1:c.*1602C>A
- XM_005245538.1:c.*1602C>A
- XM_005245693.1:c.1160+116G>T
- XM_005245693.3:c.1160+116G>T
- XM_005245694.1:c.1145+116G>T
- XM_005245694.3:c.1145+116G>T
- XM_005245695.1:c.1031+116G>T
- XM_005245696.1:c.1058+116G>T
- XM_005245697.1:c.932+116G>T
- XM_005245697.3:c.932+116G>T
- XM_005245698.1:c.*46+116G>T
- XM_005245699.1:c.*46+116G>T
- XM_006711572.1:c.*1602C>A
- XM_011510057.1:c.*1602C>A
- XM_011510237.1:c.1031+116G>T
- rs17393733
- rs386590491
- rs56504295
- rs57597870
History
No history available.