Linked Data
ClinVar Variation Id:
49317
dbSNP Id:
rs45437192
ExAC:
16:2136258 C / T
gnomAD v2:
16-2136258-C-T
gnomAD v3:
16-2086257-C-T
gnomAD v4:
16-2086257-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2086257C>T , CM000678.2:g.2086257C>T | GRCh38 |
| NC_000016.9:g.2136258C>T , CM000678.1:g.2136258C>T | GRCh37 |
| NC_000016.8:g.2076259C>T | NCBI36 |
| NG_005895.1:g.41952C>T , LRG_487:g.41952C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*3076C>T | ENSP00000455997.2:n.*3076C>T | |
| ENST00000642206.2:c.4574C>T | ENSP00000495146.2:p.Thr1525Met | |
| ENST00000642365.2:c.4724C>T | ENSP00000495459.2:p.Thr1575Met | |
| ENST00000644417.2:c.*5240C>T | ENSP00000493912.2:n.*5240C>T | |
| ENST00000646464.2:c.*7476C>T | ENSP00000496610.2:n.*7476C>T | |
| ENST00000219476.9:c.4727C>T MANE Select | ENSP00000219476.3:p.Thr1576Met | |
| ENST00000350773.9:c.4658C>T | ENSP00000344383.4:p.Thr1553Met | |
| ENST00000401874.7:c.4526C>T | ENSP00000384468.2:p.Thr1509Met | |
| ENST00000568454.6:c.4559C>T | ENSP00000454487.1:p.Thr1520Met | |
| ENST00000569110.2:c.950C>T | ||
| ENST00000569930.2:n.2609C>T | ||
| ENST00000642365.1:c.3381C>T | ||
| ENST00000642561.1:c.4598C>T | ENSP00000495099.1:p.Thr1533Met | |
| ENST00000642728.1:n.909C>T | ||
| ENST00000642791.1:n.324C>T | ||
| ENST00000642797.1:c.4529C>T | ENSP00000493846.1:p.Thr1510Met | |
| ENST00000642936.1:c.4595C>T | ENSP00000494514.1:p.Thr1532Met | |
| ENST00000643088.1:c.4520C>T | ENSP00000494747.1:p.Thr1507Met | |
| ENST00000643177.1:n.741C>T | ||
| ENST00000643426.1:n.2375C>T | ||
| ENST00000643946.1:c.4652C>T | ENSP00000495927.1:p.Thr1551Met | |
| ENST00000644043.1:c.4598C>T | ENSP00000496262.1:p.Thr1533Met | |
| ENST00000644278.1:n.209C>T | ||
| ENST00000644329.1:c.4526C>T | ENSP00000496611.1:p.Thr1509Met | |
| ENST00000644335.1:c.4523C>T | ENSP00000496317.1:p.Thr1508Met | |
| ENST00000644399.1:c.4648C>T | ||
| ENST00000645024.1:n.2811C>T | ||
| ENST00000646388.1:c.4721C>T | ENSP00000495921.1:p.Thr1574Met | |
| ENST00000646634.1:n.3542C>T | ||
| ENST00000646674.1:n.1979C>T | ||
| ENST00000647042.1:n.1950C>T | ||
| ENST00000647180.1:n.1840C>T | ||
| ENST00000219476.7:c.4727C>T | ENSP00000219476.3:p.Thr1576Met | |
| ENST00000350773.8:c.4658C>T | ENSP00000344383.4:p.Thr1553Met | |
| ENST00000382538.10:c.4382C>T | ENSP00000371978.6:p.Thr1461Met | |
| ENST00000401874.6:c.4526C>T | ENSP00000384468.2:p.Thr1509Met | |
| ENST00000439117.6:c.*3894C>T | ENSP00000406980.2:n.*3894C>T | |
| ENST00000439673.6:c.4418C>T | ENSP00000399232.2:p.Thr1473Met | |
| ENST00000497886.5:n.2485C>T | ||
| ENST00000568454.5:c.4559C>T | ENSP00000454487.1:p.Thr1520Met | |
| ENST00000569110.1:c.909C>T | ||
| ENST00000569930.1:n.1842C>T | ||
| NM_000548.3:c.4727C>T , LRG_487t1:c.4727C>T | NP_000539.2:p.Thr1576Met | |
| NM_001077183.1:c.4526C>T | NP_001070651.1:p.Thr1509Met | |
| NM_001114382.1:c.4658C>T | NP_001107854.1:p.Thr1553Met | |
| XM_005255529.3:c.4598C>T | XP_005255586.2:p.Thr1533Met | |
| XM_005255531.3:c.4529C>T | XP_005255588.2:p.Thr1510Met | |
| XM_011522636.1:c.4781C>T | XP_011520938.1:p.Thr1594Met | |
| XM_011522637.1:c.4778C>T | XP_011520939.1:p.Thr1593Met | |
| XM_011522638.1:c.4670C>T | XP_011520940.1:p.Thr1557Met | |
| XM_011522639.1:c.4652C>T | XP_011520941.1:p.Thr1551Met | |
| XM_011522640.1:c.4649C>T | XP_011520942.1:p.Thr1550Met | |
| XM_011522641.1:c.4418C>T | XP_011520943.1:p.Thr1473Met | |
| NM_000548.4:c.4727C>T | NP_000539.2:p.Thr1576Met | |
| NM_001077183.2:c.4526C>T | NP_001070651.1:p.Thr1509Met | |
| NM_001114382.2:c.4658C>T | NP_001107854.1:p.Thr1553Met | |
| NM_001318827.1:c.4418C>T | NP_001305756.1:p.Thr1473Met | |
| NM_001318829.1:c.4382C>T | NP_001305758.1:p.Thr1461Met | |
| NM_001318831.1:c.3995C>T | NP_001305760.1:p.Thr1332Met | |
| NM_001318832.1:c.4559C>T | NP_001305761.1:p.Thr1520Met | |
| NM_001363528.1:c.4529C>T | NP_001350457.1:p.Thr1510Met | |
| NM_021055.2:c.4598C>T | NP_066399.2:p.Thr1533Met | |
| XM_005255531.4:c.4529C>T | XP_005255588.2:p.Thr1510Met | |
| XM_011522636.2:c.4781C>T | XP_011520938.1:p.Thr1594Met | |
| XM_011522637.2:c.4778C>T | XP_011520939.1:p.Thr1593Met | |
| XM_011522638.2:c.4943C>T | XP_011520940.2:p.Thr1648Met | |
| XM_011522639.2:c.4652C>T | XP_011520941.1:p.Thr1551Met | |
| XM_011522640.2:c.4649C>T | XP_011520942.1:p.Thr1550Met | |
| XM_017023615.1:c.4724C>T | XP_016879104.1:p.Thr1575Met | |
| XM_017023616.1:c.4595C>T | XP_016879105.1:p.Thr1532Met | |
| XM_017023617.1:c.4691C>T | XP_016879106.1:p.Thr1564Met | |
| XM_017023618.1:c.3437C>T | XP_016879107.1:p.Thr1146Met | |
| XM_024450413.1:c.4526C>T | XP_024306181.1:p.Thr1509Met | |
| NM_000548.5:c.4727C>T MANE Select | NP_000539.2:p.Thr1576Met | |
| NM_001370404.1:c.4595C>T | NP_001357333.1:p.Thr1532Met | |
| NM_001370405.1:c.4598C>T | NP_001357334.1:p.Thr1533Met | |
| NM_001077183.3:c.4526C>T | NP_001070651.1:p.Thr1509Met | |
| NM_001114382.3:c.4658C>T | NP_001107854.1:p.Thr1553Met | |
| NM_001318827.2:c.4418C>T | NP_001305756.1:p.Thr1473Met | |
| NM_001318829.2:c.4382C>T | NP_001305758.1:p.Thr1461Met | |
| NM_001318831.2:c.3995C>T | NP_001305760.1:p.Thr1332Met | |
| NM_001318832.2:c.4559C>T | NP_001305761.1:p.Thr1520Met | |
| NM_001363528.2:c.4529C>T | NP_001350457.1:p.Thr1510Met | |
| NM_021055.3:c.4598C>T | NP_066399.2:p.Thr1533Met |