Linked Data
ClinVar Variation Id:
198449
dbSNP Id:
rs775739498
ExAC:
16:28498838 A / G
gnomAD v2:
16-28498838-A-G
gnomAD v3:
16-28487517-A-G
gnomAD v4:
16-28487517-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28487517A>G , CM000678.2:g.28487517A>G | GRCh38 |
| NC_000016.9:g.28498838A>G , CM000678.1:g.28498838A>G | GRCh37 |
| NC_000016.8:g.28406339A>G | NCBI36 |
| NG_008654.2:g.9786T>C , LRG_689:g.9786T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333496.14:c.327T>C | ENSP00000329171.9:p.Ile109= | |
| ENST00000355477.10:c.399T>C | ENSP00000347660.7:p.Ile133= | |
| ENST00000357857.14:c.237T>C | ENSP00000350523.9:p.Ile79= | |
| ENST00000359984.12:c.399T>C | ENSP00000353073.9:p.Ile133= | |
| ENST00000360019.8:c.327T>C | ENSP00000353116.3:p.Ile109= | |
| ENST00000395653.9:c.157T>C | ENSP00000379014.5:p.Leu53= | |
| ENST00000561505.2:c.85T>C | ENSP00000457615.2:p.Leu29= | |
| ENST00000561689.6:n.684T>C | ||
| ENST00000565316.6:c.399T>C | ENSP00000456117.1:p.Ile133= | |
| ENST00000565778.6:c.247T>C | ENSP00000458015.1:p.Leu83= | |
| ENST00000566083.6:n.857T>C | ||
| ENST00000566824.6:n.379T>C | ||
| ENST00000567495.6:c.399T>C | ENSP00000456013.2:p.Ile133= | |
| ENST00000567963.6:c.237T>C | ENSP00000455387.2:p.Ile79= | |
| ENST00000568076.6:n.526T>C | ||
| ENST00000568422.6:c.399T>C | ENSP00000455549.2:p.Ile133= | |
| ENST00000568443.2:c.552T>C | ENSP00000454899.2:p.Ile184= | |
| ENST00000568452.6:n.502T>C | ||
| ENST00000568472.6:n.492T>C | ||
| ENST00000568497.6:c.-293+1773T>C | ENSP00000456414.2:n.-293+1773T>C | |
| ENST00000568558.6:c.319T>C | ENSP00000455603.2:p.Leu107= | |
| ENST00000569430.7:c.399T>C | ENSP00000454229.1:p.Ile133= | |
| ENST00000628023.3:c.222+1773T>C | ENSP00000486178.1:n.222+1773T>C | |
| ENST00000635861.1:c.157T>C | ENSP00000490034.1:p.Leu53= | |
| ENST00000635887.1:c.399T>C | ENSP00000490709.1:p.Ile133= | |
| ENST00000635958.1:n.510T>C | ||
| ENST00000635973.1:c.150T>C | ENSP00000490363.1:p.Ile50= | |
| ENST00000636017.1:c.319T>C | ENSP00000490538.1:p.Leu107= | |
| ENST00000636078.1:n.441T>C | ||
| ENST00000636147.2:c.399T>C MANE Select | ENSP00000490105.1:p.Ile133= | |
| ENST00000636172.1:c.319T>C | ENSP00000490505.1:p.Leu107= | |
| ENST00000636228.1:c.237T>C | ENSP00000489627.1:p.Ile79= | |
| ENST00000636351.1:n.119T>C | ||
| ENST00000636503.1:c.399T>C | ENSP00000489824.1:p.Ile133= | |
| ENST00000636766.1:c.399T>C | ENSP00000489841.1:p.Ile133= | |
| ENST00000636839.1:n.551T>C | ||
| ENST00000636853.1:n.475T>C | ||
| ENST00000636866.1:c.399T>C | ENSP00000490880.1:p.Ile133= | |
| ENST00000636977.1:n.1467T>C | ||
| ENST00000637100.1:c.399T>C | ENSP00000490394.1:p.Ile133= | |
| ENST00000637107.1:c.472T>C | ENSP00000490248.1:p.Leu158= | |
| ENST00000637184.1:c.399T>C | ENSP00000489952.1:p.Ile133= | |
| ENST00000637299.1:c.*208T>C | ENSP00000489823.1:n.*208T>C | |
| ENST00000637376.1:c.399T>C | ENSP00000490758.1:p.Ile133= | |
| ENST00000637578.1:c.157T>C | ENSP00000490206.1:p.Leu53= | |
| ENST00000637699.1:c.399T>C | ENSP00000490049.1:p.Ile133= | |
| ENST00000637871.1:c.319T>C | ENSP00000490670.1:p.Leu107= | |
| ENST00000637985.1:c.*338T>C | ENSP00000490932.1:n.*338T>C | |
| ENST00000333496.13:c.327T>C | ENSP00000329171.9:p.Ile109= | |
| ENST00000355477.9:c.399T>C | ENSP00000347660.6:p.Ile133= | |
| ENST00000357806.11:c.319T>C | ENSP00000350457.7:p.Leu107= | |
| ENST00000357857.13:c.237T>C | ENSP00000350523.9:p.Ile79= | |
| ENST00000359984.11:c.237T>C | ENSP00000353073.8:p.Ile79= | |
| ENST00000360019.6:c.399T>C | ENSP00000353116.2:p.Ile133= | |
| ENST00000395653.8:c.99T>C | ENSP00000379014.4:p.Ile33= | |
| ENST00000561505.1:c.99T>C | ENSP00000457615.1:p.Ile33= | |
| ENST00000561689.5:n.240T>C | ||
| ENST00000563874.5:n.1753T>C | ||
| ENST00000564574.5:n.447T>C | ||
| ENST00000565047.1:n.210T>C | ||
| ENST00000565140.5:c.399T>C | ENSP00000455342.1:p.Ile133= | |
| ENST00000565316.5:c.399T>C | ENSP00000456117.1:p.Ile133= | |
| ENST00000565688.5:c.150T>C | ENSP00000456122.1:p.Ile50= | |
| ENST00000565778.5:c.247T>C | ENSP00000458015.1:p.Leu83= | |
| ENST00000566057.5:c.230T>C | ENSP00000456693.1:p.Phe77Ser | |
| ENST00000566083.5:n.630T>C | ||
| ENST00000566824.5:n.448T>C | ||
| ENST00000567495.5:c.399T>C | ENSP00000456013.1:p.Ile133= | |
| ENST00000567963.5:c.399T>C | ENSP00000455387.1:p.Ile133= | |
| ENST00000568076.5:n.399T>C | ||
| ENST00000568224.4:c.165T>C | ENSP00000454253.1:p.Ile55= | |
| ENST00000568422.5:c.179T>C | ENSP00000455549.1:p.Phe60Ser | |
| ENST00000568452.5:n.399T>C | ||
| ENST00000568472.5:n.157+1773T>C | ||
| ENST00000568497.5:c.222+1773T>C | ENSP00000456414.1:n.222+1773T>C | |
| ENST00000568558.5:c.157T>C | ENSP00000455603.1:p.Leu53= | |
| ENST00000569030.5:c.399T>C | ENSP00000454680.1:p.Ile133= | |
| ENST00000569430.5:c.399T>C | ENSP00000454229.1:p.Ile133= | |
| ENST00000628023.2:c.222+1773T>C | ENSP00000486178.1:n.222+1773T>C | |
| ENST00000631023.2:c.399T>C | ENSP00000486616.1:p.Ile133= | |
| NM_000086.2:c.399T>C , LRG_689t1:c.399T>C | NP_000077.1:p.Ile133= | |
| NM_001042432.1:c.399T>C , LRG_689t2:c.399T>C | NP_001035897.1:p.Ile133= | |
| NM_001286104.1:c.327T>C | NP_001273033.1:p.Ile109= | |
| NM_001286105.1:c.99T>C | NP_001273034.1:p.Ile33= | |
| NM_001286109.1:c.165T>C | NP_001273038.1:p.Ile55= | |
| NM_001286110.1:c.237T>C | NP_001273039.1:p.Ile79= | |
| NM_001042432.2:c.399T>C MANE Select | NP_001035897.1:p.Ile133= | |
| NM_001286104.2:c.327T>C | NP_001273033.1:p.Ile109= | |
| NM_001286105.2:c.99T>C | NP_001273034.1:p.Ile33= | |
| NM_001286109.2:c.165T>C | NP_001273038.1:p.Ile55= | |
| NM_001286110.2:c.237T>C | NP_001273039.1:p.Ile79= |