Linked Data
ClinVar Variation Id:
158406
dbSNP Id:
rs1105273
ExAC:
2:242690745 C / T
gnomAD v2:
2-242690745-C-T
gnomAD v3:
2-241751330-C-T
gnomAD v4:
2-241751330-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.241751330C>T , CM000664.2:g.241751330C>T | GRCh38 |
| NC_000002.11:g.242690745C>T , CM000664.1:g.242690745C>T | GRCh37 |
| NC_000002.10:g.242339418C>T | NCBI36 |
| NG_012012.1:g.21716C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000321264.9:c.1082C>T MANE Select | ENSP00000315351.4:p.Ala361Val | |
| ENST00000321264.8:c.1082C>T | ENSP00000315351.4:p.Ala361Val | |
| ENST00000400769.6:c.854-4519C>T | ENSP00000383580.2:n.854-4519C>T | |
| ENST00000403782.5:c.680C>T | ENSP00000384723.1:p.Ala227Val | |
| ENST00000432449.1:c.342C>T | ||
| ENST00000436747.5:c.*1398C>T | ENSP00000400212.1:n.*1398C>T | |
| ENST00000454048.1:c.185C>T | ENSP00000404596.1:p.Ala62Val | |
| ENST00000467427.5:n.389+1036C>T | ||
| ENST00000470343.5:n.563C>T | ||
| ENST00000473126.1:n.281C>T | ||
| ENST00000486953.5:n.163+1036C>T | ||
| ENST00000496252.5:n.437C>T | ||
| NM_001287249.1:c.680C>T | NP_001274178.1:p.Ala227Val | |
| NM_152783.4:c.1082C>T | NP_689996.4:p.Ala361Val | |
| NR_109778.1:n.1063-4519C>T | ||
| XM_011511734.1:c.1160C>T | XP_011510036.1:p.Ala387Val | |
| XM_011511735.1:c.1160C>T | XP_011510037.1:p.Ala387Val | |
| XM_011511736.1:c.1082C>T | XP_011510038.1:p.Ala361Val | |
| XM_011511737.1:c.1160C>T | XP_011510039.1:p.Ala387Val | |
| XM_011511742.1:c.1297C>T | XP_011510044.1:p.Arg433Cys | |
| XM_011511743.1:c.1297C>T | XP_011510045.1:p.Arg433Cys | |
| XM_011511744.1:c.1297C>T | XP_011510046.1:p.Arg433Cys | |
| XM_011511745.1:c.1160C>T | XP_011510047.1:p.Ala387Val | |
| XM_011511748.1:c.1231C>T | XP_011510050.1:p.Arg411Cys | |
| XM_011511749.1:c.1179+1036C>T | XP_011510051.1:n.1179+1036C>T | |
| XM_011511750.1:c.1160C>T | XP_011510052.1:p.Ala387Val | |
| XM_011511751.1:c.1212+751C>T | XP_011510053.1:n.1212+751C>T | |
| XM_011511753.1:c.1075+1036C>T | XP_011510055.1:n.1075+1036C>T | |
| XM_011511754.1:c.599C>T | XP_011510056.1:p.Ala200Val | |
| XM_011511755.1:c.590C>T | XP_011510057.1:p.Ala197Val | |
| XM_011511756.1:c.853+6453C>T | XP_011510058.1:n.853+6453C>T | |
| XM_011511757.1:c.*98C>T | XP_011510059.1:n.*98C>T | |
| XR_241434.3:n.1421C>T | ||
| XR_923003.1:n.1943C>T | ||
| XR_923004.1:n.1714C>T | ||
| XR_923005.1:n.1457C>T | ||
| XR_923006.1:n.1457C>T | ||
| XR_923007.1:n.1424C>T | ||
| XR_923008.1:n.1320C>T | ||
| XR_923009.1:n.1320C>T | ||
| XR_923010.1:n.1754C>T | ||
| XR_923011.1:n.1525C>T | ||
| XR_923012.1:n.1459C>T | ||
| XR_923014.1:n.1014-4519C>T | ||
| NM_001352824.1:c.521C>T | NP_001339753.1:p.Ala174Val | |
| XM_011511734.2:c.1160C>T | XP_011510036.1:p.Ala387Val | |
| XM_011511735.2:c.1160C>T | XP_011510037.1:p.Ala387Val | |
| XM_011511736.2:c.1082C>T | XP_011510038.1:p.Ala361Val | |
| XM_011511737.3:c.1160C>T | XP_011510039.1:p.Ala387Val | |
| XM_011511743.2:c.1297C>T | XP_011510045.1:p.Arg433Cys | |
| XM_011511744.2:c.1297C>T | XP_011510046.1:p.Arg433Cys | |
| XM_011511745.3:c.1160C>T | XP_011510047.1:p.Ala387Val | |
| XM_011511749.3:c.1179+1036C>T | XP_011510051.1:n.1179+1036C>T | |
| XM_011511750.3:c.1160C>T | XP_011510052.1:p.Ala387Val | |
| XM_011511751.2:c.1212+751C>T | XP_011510053.1:n.1212+751C>T | |
| XM_011511753.3:c.1075+1036C>T | XP_011510055.1:n.1075+1036C>T | |
| XM_011511756.2:c.853+6453C>T | XP_011510058.1:n.853+6453C>T | |
| XM_017004828.2:c.1082C>T | XP_016860317.1:p.Ala361Val | |
| XM_017004829.2:c.1297C>T | XP_016860318.1:p.Arg433Cys | |
| XM_017004830.2:c.1160C>T | XP_016860319.1:p.Ala387Val | |
| XM_024453102.1:c.932C>T | XP_024308870.1:p.Ala311Val | |
| XR_001738918.2:n.1456C>T | ||
| XR_001738919.2:n.1390C>T | ||
| XR_002959334.1:n.1942C>T | ||
| XR_002959335.1:n.1586C>T | ||
| XR_241434.4:n.1420C>T | ||
| XR_923004.3:n.1713C>T | ||
| XR_923005.2:n.1456C>T | ||
| XR_923007.3:n.1423C>T | ||
| XR_923009.2:n.1319C>T | ||
| XR_923010.2:n.1753C>T | ||
| XR_923011.3:n.1524C>T | ||
| XR_923012.2:n.1458C>T | ||
| XR_923014.3:n.1013-4519C>T | ||
| NM_152783.5:c.1082C>T MANE Select | NP_689996.4:p.Ala361Val | |
| NM_001287249.2:c.680C>T | NP_001274178.1:p.Ala227Val | |
| NM_001352824.2:c.521C>T | NP_001339753.1:p.Ala174Val | |
| NR_109778.2:n.1012-4519C>T |