Linked Data
ClinVar Variation Id:
207684
dbSNP Id:
rs373018205
ExAC:
16:2134608 C / G
gnomAD v2:
16-2134608-C-G
gnomAD v3:
16-2084607-C-G
gnomAD v4:
16-2084607-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2084607C>G , CM000678.2:g.2084607C>G | GRCh38 |
| NC_000016.9:g.2134608C>G , CM000678.1:g.2134608C>G | GRCh37 |
| NC_000016.8:g.2074609C>G | NCBI36 |
| NG_005895.1:g.40302C>G , LRG_487:g.40302C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2734C>G | ENSP00000455997.2:n.*2734C>G | |
| ENST00000642206.2:c.4232C>G | ENSP00000495146.2:p.Thr1411Ser | |
| ENST00000642365.2:c.4382C>G | ENSP00000495459.2:p.Thr1461Ser | |
| ENST00000644417.2:c.*4765C>G | ENSP00000493912.2:n.*4765C>G | |
| ENST00000646464.2:c.*7134C>G | ENSP00000496610.2:n.*7134C>G | |
| ENST00000219476.9:c.4385C>G MANE Select | ENSP00000219476.3:p.Thr1462Ser | |
| ENST00000350773.9:c.4316C>G | ENSP00000344383.4:p.Thr1439Ser | |
| ENST00000401874.7:c.4184C>G | ENSP00000384468.2:p.Thr1395Ser | |
| ENST00000568454.6:c.4217C>G | ENSP00000454487.1:p.Thr1406Ser | |
| ENST00000569110.2:c.621C>G | ||
| ENST00000569930.2:n.2267C>G | ||
| ENST00000642365.1:c.3039C>G | ||
| ENST00000642561.1:c.4256C>G | ENSP00000495099.1:p.Thr1419Ser | |
| ENST00000642728.1:n.567C>G | ||
| ENST00000642797.1:c.4187C>G | ENSP00000493846.1:p.Thr1396Ser | |
| ENST00000642936.1:c.4253C>G | ENSP00000494514.1:p.Thr1418Ser | |
| ENST00000643088.1:c.4184C>G | ENSP00000494747.1:p.Thr1395Ser | |
| ENST00000643177.1:n.399C>G | ||
| ENST00000643426.1:n.2033C>G | ||
| ENST00000643946.1:c.4316C>G | ENSP00000495927.1:p.Thr1439Ser | |
| ENST00000644043.1:c.4256C>G | ENSP00000496262.1:p.Thr1419Ser | |
| ENST00000644329.1:c.4184C>G | ENSP00000496611.1:p.Thr1395Ser | |
| ENST00000644335.1:c.4187C>G | ENSP00000496317.1:p.Thr1396Ser | |
| ENST00000644399.1:c.4306C>G | ||
| ENST00000645024.1:n.2469C>G | ||
| ENST00000646388.1:c.4385C>G | ENSP00000495921.1:p.Thr1462Ser | |
| ENST00000646634.1:n.3200C>G | ||
| ENST00000646674.1:n.1637C>G | ||
| ENST00000647042.1:n.1608C>G | ||
| ENST00000647180.1:n.1498C>G | ||
| ENST00000219476.7:c.4385C>G | ENSP00000219476.3:p.Thr1462Ser | |
| ENST00000350773.8:c.4316C>G | ENSP00000344383.4:p.Thr1439Ser | |
| ENST00000382538.10:c.4040C>G | ENSP00000371978.6:p.Thr1347Ser | |
| ENST00000401874.6:c.4184C>G | ENSP00000384468.2:p.Thr1395Ser | |
| ENST00000439117.6:c.*3552C>G | ENSP00000406980.2:n.*3552C>G | |
| ENST00000439673.6:c.4076C>G | ENSP00000399232.2:p.Thr1359Ser | |
| ENST00000497886.5:n.2143C>G | ||
| ENST00000568454.5:c.4217C>G | ENSP00000454487.1:p.Thr1406Ser | |
| ENST00000569110.1:c.567C>G | ||
| ENST00000569930.1:n.1500C>G | ||
| NM_000548.3:c.4385C>G , LRG_487t1:c.4385C>G | NP_000539.2:p.Thr1462Ser | |
| NM_001077183.1:c.4184C>G | NP_001070651.1:p.Thr1395Ser | |
| NM_001114382.1:c.4316C>G | NP_001107854.1:p.Thr1439Ser | |
| XM_005255529.3:c.4256C>G | XP_005255586.2:p.Thr1419Ser | |
| XM_005255531.3:c.4187C>G | XP_005255588.2:p.Thr1396Ser | |
| XM_011522636.1:c.4439C>G | XP_011520938.1:p.Thr1480Ser | |
| XM_011522637.1:c.4436C>G | XP_011520939.1:p.Thr1479Ser | |
| XM_011522638.1:c.4328C>G | XP_011520940.1:p.Thr1443Ser | |
| XM_011522639.1:c.4310C>G | XP_011520941.1:p.Thr1437Ser | |
| XM_011522640.1:c.4307C>G | XP_011520942.1:p.Thr1436Ser | |
| XM_011522641.1:c.4076C>G | XP_011520943.1:p.Thr1359Ser | |
| NM_000548.4:c.4385C>G | NP_000539.2:p.Thr1462Ser | |
| NM_001077183.2:c.4184C>G | NP_001070651.1:p.Thr1395Ser | |
| NM_001114382.2:c.4316C>G | NP_001107854.1:p.Thr1439Ser | |
| NM_001318827.1:c.4076C>G | NP_001305756.1:p.Thr1359Ser | |
| NM_001318829.1:c.4040C>G | NP_001305758.1:p.Thr1347Ser | |
| NM_001318831.1:c.3653C>G | NP_001305760.1:p.Thr1218Ser | |
| NM_001318832.1:c.4217C>G | NP_001305761.1:p.Thr1406Ser | |
| NM_001363528.1:c.4187C>G | NP_001350457.1:p.Thr1396Ser | |
| NM_021055.2:c.4256C>G | NP_066399.2:p.Thr1419Ser | |
| XM_005255531.4:c.4187C>G | XP_005255588.2:p.Thr1396Ser | |
| XM_011522636.2:c.4439C>G | XP_011520938.1:p.Thr1480Ser | |
| XM_011522637.2:c.4436C>G | XP_011520939.1:p.Thr1479Ser | |
| XM_011522638.2:c.4601C>G | XP_011520940.2:p.Thr1534Ser | |
| XM_011522639.2:c.4310C>G | XP_011520941.1:p.Thr1437Ser | |
| XM_011522640.2:c.4307C>G | XP_011520942.1:p.Thr1436Ser | |
| XM_017023615.1:c.4382C>G | XP_016879104.1:p.Thr1461Ser | |
| XM_017023616.1:c.4253C>G | XP_016879105.1:p.Thr1418Ser | |
| XM_017023617.1:c.4349C>G | XP_016879106.1:p.Thr1450Ser | |
| XM_017023618.1:c.3095C>G | XP_016879107.1:p.Thr1032Ser | |
| XM_024450413.1:c.4184C>G | XP_024306181.1:p.Thr1395Ser | |
| NM_000548.5:c.4385C>G MANE Select | NP_000539.2:p.Thr1462Ser | |
| NM_001370404.1:c.4253C>G | NP_001357333.1:p.Thr1418Ser | |
| NM_001370405.1:c.4256C>G | NP_001357334.1:p.Thr1419Ser | |
| NM_001077183.3:c.4184C>G | NP_001070651.1:p.Thr1395Ser | |
| NM_001114382.3:c.4316C>G | NP_001107854.1:p.Thr1439Ser | |
| NM_001318827.2:c.4076C>G | NP_001305756.1:p.Thr1359Ser | |
| NM_001318829.2:c.4040C>G | NP_001305758.1:p.Thr1347Ser | |
| NM_001318831.2:c.3653C>G | NP_001305760.1:p.Thr1218Ser | |
| NM_001318832.2:c.4217C>G | NP_001305761.1:p.Thr1406Ser | |
| NM_001363528.2:c.4187C>G | NP_001350457.1:p.Thr1396Ser | |
| NM_021055.3:c.4256C>G | NP_066399.2:p.Thr1419Ser |