Linked Data
ClinVar Variation Id:
1122761
dbSNP Id:
rs748404138
gnomAD v2:
7-6022481-G-C
gnomAD v4:
7-5982850-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5982850G>C , CM000669.2:g.5982850G>C | GRCh38 |
| NC_000007.13:g.6022481G>C , CM000669.1:g.6022481G>C | GRCh37 |
| NC_000007.12:g.5989007G>C | NCBI36 |
| NG_008466.1:g.31257C>G , LRG_161:g.31257C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699814.2:c.*1544C>G | ENSP00000514615.2:n.*1544C>G | |
| ENST00000699840.2:c.2145C>G | ENSP00000514638.2:p.Thr715= | |
| ENST00000699930.2:c.2040C>G | ENSP00000514695.2:p.Thr680= | |
| ENST00000406569.8:c.1678+4237C>G | ENSP00000514464.1:n.1678+4237C>G | |
| ENST00000644110.2:c.*1742C>G | ENSP00000496392.2:n.*1742C>G | |
| ENST00000699752.1:c.1992C>G | ENSP00000514561.1:p.Thr664= | |
| ENST00000699753.1:c.*1569C>G | ENSP00000514562.1:n.*1569C>G | |
| ENST00000699754.1:c.1950C>G | ENSP00000514563.1:p.Thr650= | |
| ENST00000699755.1:c.*1547C>G | ENSP00000514564.1:n.*1547C>G | |
| ENST00000699756.1:c.*1735C>G | ENSP00000514565.1:n.*1735C>G | |
| ENST00000699757.1:c.*1405C>G | ENSP00000514566.1:n.*1405C>G | |
| ENST00000699758.1:c.*1405C>G | ENSP00000514567.1:n.*1405C>G | |
| ENST00000699759.1:n.3002C>G | ||
| ENST00000699760.1:c.1830C>G | ENSP00000514568.1:p.Thr610= | |
| ENST00000699761.1:c.1743C>G | ENSP00000514569.1:p.Thr581= | |
| ENST00000699762.1:c.1575C>G | ENSP00000514570.1:p.Thr525= | |
| ENST00000699763.1:c.*1238C>G | ENSP00000514571.1:n.*1238C>G | |
| ENST00000699764.1:c.*466C>G | ENSP00000514572.1:n.*466C>G | |
| ENST00000699765.1:c.*1244C>G | ENSP00000514573.1:n.*1244C>G | |
| ENST00000699766.1:c.2148C>G | ENSP00000514574.1:p.Thr716= | |
| ENST00000699767.1:c.2148C>G | ENSP00000514575.1:p.Thr716= | |
| ENST00000699768.1:c.2148C>G | ENSP00000514576.1:p.Thr716= | |
| ENST00000699811.1:c.1743C>G | ENSP00000514614.1:p.Thr581= | |
| ENST00000699813.1:n.2261C>G | ||
| ENST00000699814.1:c.1771C>G | ||
| ENST00000699815.1:c.*1679C>G | ENSP00000514616.1:n.*1679C>G | |
| ENST00000699816.1:c.*1038C>G | ENSP00000514617.1:n.*1038C>G | |
| ENST00000699817.1:c.*1742C>G | ENSP00000514618.1:n.*1742C>G | |
| ENST00000699818.1:c.1743C>G | ENSP00000514619.1:p.Thr581= | |
| ENST00000699819.1:c.*1305C>G | ENSP00000514620.1:n.*1305C>G | |
| ENST00000699820.1:c.*86C>G | ENSP00000514621.1:n.*86C>G | |
| ENST00000699821.1:c.1743C>G | ENSP00000514622.1:p.Thr581= | |
| ENST00000699822.1:c.*1600C>G | ENSP00000514623.1:n.*1600C>G | |
| ENST00000699823.1:c.1743C>G | ENSP00000514624.1:p.Thr581= | |
| ENST00000699824.1:c.*1651C>G | ENSP00000514625.1:n.*1651C>G | |
| ENST00000699825.1:c.1587C>G | ENSP00000514626.1:p.Thr529= | |
| ENST00000699826.1:c.*1547C>G | ENSP00000514627.1:n.*1547C>G | |
| ENST00000699827.1:c.1980C>G | ENSP00000514628.1:p.Thr660= | |
| ENST00000699828.1:c.*1238C>G | ENSP00000514629.1:n.*1238C>G | |
| ENST00000699833.1:n.3920C>G | ||
| ENST00000699837.1:c.1743C>G | ENSP00000514635.1:p.Thr581= | |
| ENST00000699838.1:c.*2048C>G | ENSP00000514636.1:n.*2048C>G | |
| ENST00000699839.1:c.2334C>G | ENSP00000514637.1:p.Thr778= | |
| ENST00000699916.1:c.*1405C>G | ENSP00000514684.1:n.*1405C>G | |
| ENST00000699917.1:c.*1597C>G | ENSP00000514685.1:n.*1597C>G | |
| ENST00000699918.1:c.*1649C>G | ENSP00000514686.1:n.*1649C>G | |
| ENST00000699919.1:c.*1735C>G | ENSP00000514687.1:n.*1735C>G | |
| ENST00000699920.1:c.*1784C>G | ENSP00000514688.1:n.*1784C>G | |
| ENST00000699928.1:c.*86C>G | ENSP00000514693.1:n.*86C>G | |
| ENST00000699951.1:c.*1244C>G | ENSP00000514706.1:n.*1244C>G | |
| ENST00000699952.1:c.804-9308C>G | ENSP00000514707.1:n.804-9308C>G | |
| ENST00000265849.12:c.2148C>G MANE Select | ENSP00000265849.7:p.Thr716= | |
| ENST00000642292.1:c.1743C>G | ENSP00000495524.1:p.Thr581= | |
| ENST00000642456.1:c.1743C>G | ENSP00000493814.1:p.Thr581= | |
| ENST00000643595.1:c.*1547C>G | ENSP00000494497.1:n.*1547C>G | |
| ENST00000644110.1:c.1830C>G | ENSP00000496392.1:p.Thr610= | |
| ENST00000265849.11:c.2148C>G | ENSP00000265849.7:p.Thr716= | |
| ENST00000382321.5:c.945C>G | ENSP00000371758.4:p.Thr315= | |
| ENST00000406569.7:n.1678+4237C>G | ||
| ENST00000441476.6:c.1830C>G | ENSP00000392843.2:p.Thr610= | |
| NM_000535.5:c.2148C>G , LRG_161t1:c.2148C>G | NP_000526.1:p.Thr716= | |
| NR_003085.2:n.2230C>G | ||
| XM_006715742.2:c.2142C>G | XP_006715805.1:p.Thr714= | |
| XM_006715744.2:c.1215C>G | XP_006715807.1:p.Thr405= | |
| XM_011515427.1:c.2193C>G | XP_011513729.1:p.Thr731= | |
| XM_011515428.1:c.2037C>G | XP_011513730.1:p.Thr679= | |
| XM_011515429.1:c.1830C>G | XP_011513731.1:p.Thr610= | |
| XM_011515430.1:c.1830C>G | XP_011513732.1:p.Thr610= | |
| NM_000535.6:c.2148C>G | NP_000526.2:p.Thr716= | |
| NM_001322003.1:c.1743C>G | NP_001308932.1:p.Thr581= | |
| NM_001322004.1:c.1743C>G | NP_001308933.1:p.Thr581= | |
| NM_001322005.1:c.1743C>G | NP_001308934.1:p.Thr581= | |
| NM_001322006.1:c.1992C>G | NP_001308935.1:p.Thr664= | |
| NM_001322007.1:c.1830C>G | NP_001308936.1:p.Thr610= | |
| NM_001322008.1:c.1830C>G | NP_001308937.1:p.Thr610= | |
| NM_001322009.1:c.1743C>G | NP_001308938.1:p.Thr581= | |
| NM_001322010.1:c.1587C>G | NP_001308939.1:p.Thr529= | |
| NM_001322011.1:c.1215C>G | NP_001308940.1:p.Thr405= | |
| NM_001322012.1:c.1215C>G | NP_001308941.1:p.Thr405= | |
| NM_001322013.1:c.1575C>G | NP_001308942.1:p.Thr525= | |
| NM_001322014.1:c.2148C>G | NP_001308943.1:p.Thr716= | |
| NM_001322015.1:c.1839C>G | NP_001308944.1:p.Thr613= | |
| NR_136154.1:n.2235C>G | ||
| XM_006715744.4:c.1215C>G | XP_006715807.1:p.Thr405= | |
| XM_017012342.2:c.1215C>G | XP_016867831.1:p.Thr405= | |
| XM_024446800.1:c.1587C>G | XP_024302568.1:p.Thr529= | |
| NM_000535.7:c.2148C>G MANE Select | NP_000526.2:p.Thr716= | |
| NM_001322003.2:c.1743C>G | NP_001308932.1:p.Thr581= | |
| NM_001322004.2:c.1743C>G | NP_001308933.1:p.Thr581= | |
| NM_001322005.2:c.1743C>G | NP_001308934.1:p.Thr581= | |
| NM_001322006.2:c.1992C>G | NP_001308935.1:p.Thr664= | |
| NM_001322008.2:c.1830C>G | NP_001308937.1:p.Thr610= | |
| NM_001322009.2:c.1743C>G | NP_001308938.1:p.Thr581= | |
| NM_001322010.2:c.1587C>G | NP_001308939.1:p.Thr529= | |
| NM_001322011.2:c.1215C>G | NP_001308940.1:p.Thr405= | |
| NM_001322012.2:c.1215C>G | NP_001308941.1:p.Thr405= | |
| NM_001322013.2:c.1575C>G | NP_001308942.1:p.Thr525= | |
| NM_001322014.2:c.2148C>G | NP_001308943.1:p.Thr716= | |
| NM_001322015.2:c.1839C>G | NP_001308944.1:p.Thr613= | |
| NM_001322007.2:c.1830C>G | NP_001308936.1:p.Thr610= |