MyVariant.info:
GRCh37
chr16:g.2134552T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2084551T>C , CM000678.2:g.2084551T>C | GRCh38 |
| NC_000016.9:g.2134552T>C , CM000678.1:g.2134552T>C | GRCh37 |
| NC_000016.8:g.2074553T>C | NCBI36 |
| NG_005895.1:g.40246T>C , LRG_487:g.40246T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2678T>C | ENSP00000455997.2:n.*2678T>C | |
| ENST00000642206.2:c.4176T>C | ENSP00000495146.2:p.Gly1392= | |
| ENST00000642365.2:c.4326T>C | ENSP00000495459.2:p.Gly1442= | |
| ENST00000644417.2:c.*4709T>C | ENSP00000493912.2:n.*4709T>C | |
| ENST00000646464.2:c.*7078T>C | ENSP00000496610.2:n.*7078T>C | |
| ENST00000219476.9:c.4329T>C MANE Select | ENSP00000219476.3:p.Gly1443= | |
| ENST00000350773.9:c.4260T>C | ENSP00000344383.4:p.Gly1420= | |
| ENST00000401874.7:c.4128T>C | ENSP00000384468.2:p.Gly1376= | |
| ENST00000568454.6:c.4161T>C | ENSP00000454487.1:p.Gly1387= | |
| ENST00000569110.2:c.565T>C | ||
| ENST00000569930.2:n.2211T>C | ||
| ENST00000642365.1:c.2983T>C | ||
| ENST00000642561.1:c.4200T>C | ENSP00000495099.1:p.Gly1400= | |
| ENST00000642728.1:n.511T>C | ||
| ENST00000642797.1:c.4131T>C | ENSP00000493846.1:p.Gly1377= | |
| ENST00000642936.1:c.4197T>C | ENSP00000494514.1:p.Gly1399= | |
| ENST00000643088.1:c.4128T>C | ENSP00000494747.1:p.Gly1376= | |
| ENST00000643177.1:n.343T>C | ||
| ENST00000643426.1:n.1977T>C | ||
| ENST00000643946.1:c.4260T>C | ENSP00000495927.1:p.Gly1420= | |
| ENST00000644043.1:c.4200T>C | ENSP00000496262.1:p.Gly1400= | |
| ENST00000644329.1:c.4128T>C | ENSP00000496611.1:p.Gly1376= | |
| ENST00000644335.1:c.4131T>C | ENSP00000496317.1:p.Gly1377= | |
| ENST00000644399.1:c.4250T>C | ||
| ENST00000645024.1:n.2413T>C | ||
| ENST00000646388.1:c.4329T>C | ENSP00000495921.1:p.Gly1443= | |
| ENST00000646634.1:n.3144T>C | ||
| ENST00000646674.1:n.1581T>C | ||
| ENST00000647042.1:n.1552T>C | ||
| ENST00000647180.1:n.1442T>C | ||
| ENST00000219476.7:c.4329T>C | ENSP00000219476.3:p.Gly1443= | |
| ENST00000350773.8:c.4260T>C | ENSP00000344383.4:p.Gly1420= | |
| ENST00000382538.10:c.3984T>C | ENSP00000371978.6:p.Gly1328= | |
| ENST00000401874.6:c.4128T>C | ENSP00000384468.2:p.Gly1376= | |
| ENST00000439117.6:c.*3496T>C | ENSP00000406980.2:n.*3496T>C | |
| ENST00000439673.6:c.4020T>C | ENSP00000399232.2:p.Gly1340= | |
| ENST00000497886.5:n.2087T>C | ||
| ENST00000568454.5:c.4161T>C | ENSP00000454487.1:p.Gly1387= | |
| ENST00000569110.1:c.511T>C | ||
| ENST00000569930.1:n.1444T>C | ||
| NM_000548.3:c.4329T>C , LRG_487t1:c.4329T>C | NP_000539.2:p.Gly1443= | |
| NM_001077183.1:c.4128T>C | NP_001070651.1:p.Gly1376= | |
| NM_001114382.1:c.4260T>C | NP_001107854.1:p.Gly1420= | |
| XM_005255529.3:c.4200T>C | XP_005255586.2:p.Gly1400= | |
| XM_005255531.3:c.4131T>C | XP_005255588.2:p.Gly1377= | |
| XM_011522636.1:c.4383T>C | XP_011520938.1:p.Gly1461= | |
| XM_011522637.1:c.4380T>C | XP_011520939.1:p.Gly1460= | |
| XM_011522638.1:c.4272T>C | XP_011520940.1:p.Gly1424= | |
| XM_011522639.1:c.4254T>C | XP_011520941.1:p.Gly1418= | |
| XM_011522640.1:c.4251T>C | XP_011520942.1:p.Gly1417= | |
| XM_011522641.1:c.4020T>C | XP_011520943.1:p.Gly1340= | |
| NM_000548.4:c.4329T>C | NP_000539.2:p.Gly1443= | |
| NM_001077183.2:c.4128T>C | NP_001070651.1:p.Gly1376= | |
| NM_001114382.2:c.4260T>C | NP_001107854.1:p.Gly1420= | |
| NM_001318827.1:c.4020T>C | NP_001305756.1:p.Gly1340= | |
| NM_001318829.1:c.3984T>C | NP_001305758.1:p.Gly1328= | |
| NM_001318831.1:c.3597T>C | NP_001305760.1:p.Gly1199= | |
| NM_001318832.1:c.4161T>C | NP_001305761.1:p.Gly1387= | |
| NM_001363528.1:c.4131T>C | NP_001350457.1:p.Gly1377= | |
| NM_021055.2:c.4200T>C | NP_066399.2:p.Gly1400= | |
| XM_005255531.4:c.4131T>C | XP_005255588.2:p.Gly1377= | |
| XM_011522636.2:c.4383T>C | XP_011520938.1:p.Gly1461= | |
| XM_011522637.2:c.4380T>C | XP_011520939.1:p.Gly1460= | |
| XM_011522638.2:c.4545T>C | XP_011520940.2:p.Gly1515= | |
| XM_011522639.2:c.4254T>C | XP_011520941.1:p.Gly1418= | |
| XM_011522640.2:c.4251T>C | XP_011520942.1:p.Gly1417= | |
| XM_017023615.1:c.4326T>C | XP_016879104.1:p.Gly1442= | |
| XM_017023616.1:c.4197T>C | XP_016879105.1:p.Gly1399= | |
| XM_017023617.1:c.4293T>C | XP_016879106.1:p.Gly1431= | |
| XM_017023618.1:c.3039T>C | XP_016879107.1:p.Gly1013= | |
| XM_024450413.1:c.4128T>C | XP_024306181.1:p.Gly1376= | |
| NM_000548.5:c.4329T>C MANE Select | NP_000539.2:p.Gly1443= | |
| NM_001370404.1:c.4197T>C | NP_001357333.1:p.Gly1399= | |
| NM_001370405.1:c.4200T>C | NP_001357334.1:p.Gly1400= | |
| NM_001077183.3:c.4128T>C | NP_001070651.1:p.Gly1376= | |
| NM_001114382.3:c.4260T>C | NP_001107854.1:p.Gly1420= | |
| NM_001318827.2:c.4020T>C | NP_001305756.1:p.Gly1340= | |
| NM_001318829.2:c.3984T>C | NP_001305758.1:p.Gly1328= | |
| NM_001318831.2:c.3597T>C | NP_001305760.1:p.Gly1199= | |
| NM_001318832.2:c.4161T>C | NP_001305761.1:p.Gly1387= | |
| NM_001363528.2:c.4131T>C | NP_001350457.1:p.Gly1377= | |
| NM_021055.3:c.4200T>C | NP_066399.2:p.Gly1400= |