Linked Data
ClinVar Variation Id:
166897
dbSNP Id:
rs727503872
gnomAD v2:
9-134394777-C-T
gnomAD v3:
9-131519390-C-T
gnomAD v4:
9-131519390-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131519390C>T , CM000671.2:g.131519390C>T | GRCh38 |
| NC_000009.11:g.134394777C>T , CM000671.1:g.134394777C>T | GRCh37 |
| NC_000009.10:g.133384598C>T | NCBI36 |
| NG_008896.1:g.21489C>T | |
| NG_008896.2:g.21489C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.1326C>T | ENSP00000343034.7:p.Ser442= | |
| ENST00000404875.7:n.2028C>T | ||
| ENST00000423007.6:c.1545C>T | ENSP00000404119.2:p.Ser515= | |
| ENST00000677295.2:c.*1832C>T | ENSP00000504346.2:n.*1832C>T | |
| ENST00000678264.2:c.*1671C>T | ENSP00000503157.2:n.*1671C>T | |
| ENST00000682070.1:n.1953C>T | ||
| ENST00000682813.1:n.1892C>T | ||
| ENST00000683392.1:n.4235C>T | ||
| ENST00000683712.1:n.1893C>T | ||
| ENST00000683900.1:n.3388C>T | ||
| ENST00000684062.1:n.2154C>T | ||
| ENST00000684579.1:n.3334C>T | ||
| ENST00000684679.1:n.715C>T | ||
| ENST00000341012.12:c.1326C>T | ENSP00000343034.7:p.Ser442= | |
| ENST00000372220.5:c.357C>T | ENSP00000361294.5:p.Ser119= | |
| ENST00000372228.9:c.1554C>T | ENSP00000361302.3:p.Ser518= | |
| ENST00000402686.8:c.1488C>T MANE Select | ENSP00000385797.4:p.Ser496= | |
| ENST00000676640.1:c.1488C>T | ENSP00000503281.1:p.Ser496= | |
| ENST00000676803.1:c.663C>T | ENSP00000503093.1:p.Ser221= | |
| ENST00000676835.1:c.*703C>T | ENSP00000502911.1:n.*703C>T | |
| ENST00000677029.1:c.1032C>T | ENSP00000502936.1:p.Ser344= | |
| ENST00000677099.1:c.*1198C>T | ENSP00000504553.1:n.*1198C>T | |
| ENST00000677216.1:c.1137C>T | ENSP00000503772.1:p.Ser379= | |
| ENST00000677221.1:n.513C>T | ||
| ENST00000677295.1:c.*865C>T | ENSP00000504346.1:n.*865C>T | |
| ENST00000677444.1:c.1433C>T | ||
| ENST00000677586.1:n.969C>T | ||
| ENST00000677626.1:c.1137C>T | ENSP00000503552.1:p.Ser379= | |
| ENST00000677677.1:n.1448C>T | ||
| ENST00000677853.1:c.*496C>T | ENSP00000503488.1:n.*496C>T | |
| ENST00000678202.1:n.647C>T | ||
| ENST00000678264.1:c.*865C>T | ENSP00000503157.1:n.*865C>T | |
| ENST00000678303.1:c.1398C>T | ENSP00000503696.1:p.Ser466= | |
| ENST00000678366.1:c.*1737C>T | ENSP00000504353.1:n.*1737C>T | |
| ENST00000678546.1:c.*1433C>T | ENSP00000503062.1:n.*1433C>T | |
| ENST00000678548.1:c.*1560C>T | ENSP00000503934.1:n.*1560C>T | |
| ENST00000678626.1:n.1324C>T | ||
| ENST00000678733.1:c.569C>T | ||
| ENST00000678739.1:c.*1813-4C>T | ENSP00000503806.1:n.*1813-4C>T | |
| ENST00000678833.1:c.*1240C>T | ENSP00000503893.1:n.*1240C>T | |
| ENST00000679023.1:c.1326C>T | ENSP00000503718.1:p.Ser442= | |
| ENST00000679076.1:c.1107C>T | ||
| ENST00000679111.1:c.*244C>T | ENSP00000504257.1:n.*244C>T | |
| ENST00000679189.1:c.1137C>T | ENSP00000503356.1:p.Ser379= | |
| ENST00000341012.11:c.1326C>T | ENSP00000343034.7:p.Ser442= | |
| ENST00000372220.4:c.351C>T | ENSP00000361294.4:p.Ser117= | |
| ENST00000372228.7:c.1554C>T | ENSP00000361302.3:p.Ser518= | |
| ENST00000402686.7:c.1488C>T | ENSP00000385797.3:p.Ser496= | |
| ENST00000404875.6:c.1137C>T | ENSP00000384531.2:p.Ser379= | |
| ENST00000423007.5:c.1488C>T | ENSP00000404119.1:p.Ser496= | |
| ENST00000467848.1:n.192C>T | ||
| ENST00000485278.5:n.2042-4C>T | ||
| NM_001077365.1:c.1488C>T | NP_001070833.1:p.Ser496= | |
| NM_001077366.1:c.1326C>T | NP_001070834.1:p.Ser442= | |
| NM_001136113.1:c.1488C>T | NP_001129585.1:p.Ser496= | |
| NM_001136114.1:c.1137C>T | NP_001129586.1:p.Ser379= | |
| NM_007171.3:c.1554C>T | NP_009102.3:p.Ser518= | |
| XM_005272156.1:c.1554C>T | XP_005272213.1:p.Ser518= | |
| XM_005272158.1:c.1392C>T | XP_005272215.1:p.Ser464= | |
| XM_005272159.1:c.1203C>T | XP_005272216.1:p.Ser401= | |
| XM_005272162.1:c.357C>T | XP_005272219.1:p.Ser119= | |
| XM_006716932.1:c.1203C>T | XP_006716995.1:p.Ser401= | |
| XM_011518140.1:c.1407C>T | XP_011516442.1:p.Ser469= | |
| XM_011518141.1:c.1341C>T | XP_011516443.1:p.Ser447= | |
| XM_011518142.1:c.1245C>T | XP_011516444.1:p.Ser415= | |
| XM_011518143.1:c.1239C>T | XP_011516445.1:p.Ser413= | |
| XM_011518145.1:c.1098C>T | XP_011516447.1:p.Ser366= | |
| XM_011518147.1:c.426C>T | XP_011516449.1:p.Ser142= | |
| XR_929703.1:n.1730C>T | ||
| NM_001353193.1:c.1554C>T | NP_001340122.1:p.Ser518= | |
| NM_001353194.1:c.1326C>T | NP_001340123.1:p.Ser442= | |
| NM_001353195.1:c.1137C>T | NP_001340124.1:p.Ser379= | |
| NM_001353196.1:c.1398C>T | NP_001340125.1:p.Ser466= | |
| NM_001353197.1:c.1392C>T | NP_001340126.1:p.Ser464= | |
| NM_001353198.1:c.1392C>T | NP_001340127.1:p.Ser464= | |
| NM_001353199.1:c.1203C>T | NP_001340128.1:p.Ser401= | |
| NM_001353200.1:c.1032C>T | NP_001340129.1:p.Ser344= | |
| NR_148391.1:n.1538C>T | ||
| NR_148392.1:n.1756C>T | ||
| NR_148393.1:n.1677C>T | ||
| NR_148394.1:n.1431C>T | ||
| NR_148395.1:n.1829C>T | ||
| NR_148396.1:n.1463C>T | ||
| NR_148397.1:n.1588C>T | ||
| NR_148398.1:n.1543C>T | ||
| NR_148399.1:n.2069C>T | ||
| NR_148400.1:n.1668C>T | ||
| XM_005272162.3:c.357C>T | XP_005272219.1:p.Ser119= | |
| XM_006716932.2:c.1203C>T | XP_006716995.1:p.Ser401= | |
| XM_011518140.2:c.1407C>T | XP_011516442.1:p.Ser469= | |
| XM_011518141.2:c.1341C>T | XP_011516443.1:p.Ser447= | |
| XM_011518142.2:c.1245C>T | XP_011516444.1:p.Ser415= | |
| XM_011518143.2:c.1239C>T | XP_011516445.1:p.Ser413= | |
| XM_011518145.2:c.1098C>T | XP_011516447.1:p.Ser366= | |
| XM_017014205.2:c.357C>T | XP_016869694.1:p.Ser119= | |
| XM_024447380.1:c.357C>T | XP_024303148.1:p.Ser119= | |
| XM_024447381.1:c.663C>T | XP_024303149.1:p.Ser221= | |
| XM_024447382.1:c.357C>T | XP_024303150.1:p.Ser119= | |
| XR_001746160.2:n.1658C>T | ||
| XR_001746162.2:n.1863C>T | ||
| XR_001746164.1:n.1580C>T | ||
| XR_001746166.2:n.1875C>T | ||
| NM_001077365.2:c.1488C>T MANE Select | NP_001070833.1:p.Ser496= | |
| NM_001077366.2:c.1326C>T | NP_001070834.1:p.Ser442= | |
| NM_001136113.2:c.1488C>T | NP_001129585.1:p.Ser496= | |
| NM_001136114.2:c.1137C>T | NP_001129586.1:p.Ser379= | |
| NM_001353193.2:c.1554C>T | NP_001340122.2:p.Ser518= | |
| NM_001353194.2:c.1326C>T | NP_001340123.1:p.Ser442= | |
| NM_001353195.2:c.1137C>T | NP_001340124.1:p.Ser379= | |
| NM_001353196.2:c.1398C>T | NP_001340125.1:p.Ser466= | |
| NM_001353197.2:c.1392C>T | NP_001340126.2:p.Ser464= | |
| NM_001353198.2:c.1392C>T | NP_001340127.2:p.Ser464= | |
| NM_001353199.2:c.1203C>T | NP_001340128.2:p.Ser401= | |
| NM_001353200.2:c.1032C>T | NP_001340129.1:p.Ser344= | |
| NM_001374689.1:c.1476C>T | NP_001361618.1:p.Ser492= | |
| NM_001374690.1:c.1366-690C>T | NP_001361619.1:n.1366-690C>T | |
| NM_001374691.1:c.1137C>T | NP_001361620.1:p.Ser379= | |
| NM_001374692.1:c.1137C>T | NP_001361621.1:p.Ser379= | |
| NM_001374693.1:c.1137C>T | NP_001361622.1:p.Ser379= | |
| NM_001374695.1:c.1098C>T | NP_001361624.1:p.Ser366= | |
| NM_007171.4:c.1554C>T | NP_009102.4:p.Ser518= | |
| NR_148391.2:n.1522C>T | ||
| NR_148392.2:n.1740C>T | ||
| NR_148393.2:n.1661C>T | ||
| NR_148394.2:n.1415C>T | ||
| NR_148395.2:n.1813C>T | ||
| NR_148396.2:n.1447C>T | ||
| NR_148397.2:n.1572C>T | ||
| NR_148398.2:n.1527C>T | ||
| NR_148399.2:n.2053C>T | ||
| NR_148400.2:n.1652C>T |