Linked Data
ClinVar Variation Id:
195503
dbSNP Id:
rs138902646
ExAC:
9:134398412 C / T
gnomAD v2:
9-134398412-C-T
gnomAD v3:
9-131523025-C-T
gnomAD v4:
9-131523025-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131523025C>T , CM000671.2:g.131523025C>T | GRCh38 |
| NC_000009.11:g.134398412C>T , CM000671.1:g.134398412C>T | GRCh37 |
| NC_000009.10:g.133388233C>T | NCBI36 |
| NG_008896.1:g.25124C>T | |
| NG_008896.2:g.25124C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.1935C>T | ENSP00000343034.7:p.Tyr645= | |
| ENST00000404875.7:n.2637C>T | ||
| ENST00000423007.6:c.2154C>T | ENSP00000404119.2:p.Tyr718= | |
| ENST00000677295.2:c.*2441C>T | ENSP00000504346.2:n.*2441C>T | |
| ENST00000678264.2:c.*2280C>T | ENSP00000503157.2:n.*2280C>T | |
| ENST00000682070.1:n.2407C>T | ||
| ENST00000682639.1:c.94C>T | ||
| ENST00000682813.1:n.2494C>T | ||
| ENST00000683231.1:c.94C>T | ||
| ENST00000683392.1:n.4689C>T | ||
| ENST00000683712.1:n.2502C>T | ||
| ENST00000683900.1:n.3997C>T | ||
| ENST00000684062.1:n.2763C>T | ||
| ENST00000684399.1:c.94C>T | ||
| ENST00000684579.1:n.3943C>T | ||
| ENST00000341012.12:c.1935C>T | ENSP00000343034.7:p.Tyr645= | |
| ENST00000372220.5:c.966C>T | ENSP00000361294.5:p.Tyr322= | |
| ENST00000372228.9:c.2163C>T | ENSP00000361302.3:p.Tyr721= | |
| ENST00000402686.8:c.2097C>T MANE Select | ENSP00000385797.4:p.Tyr699= | |
| ENST00000676640.1:c.2097C>T | ENSP00000503281.1:p.Tyr699= | |
| ENST00000676803.1:c.1158C>T | ENSP00000503093.1:p.Tyr386= | |
| ENST00000676835.1:c.*1312C>T | ENSP00000502911.1:n.*1312C>T | |
| ENST00000677029.1:c.1641C>T | ENSP00000502936.1:p.Tyr547= | |
| ENST00000677099.1:c.*1807C>T | ENSP00000504553.1:n.*1807C>T | |
| ENST00000677216.1:c.1746C>T | ENSP00000503772.1:p.Tyr582= | |
| ENST00000677295.1:c.*1319C>T | ENSP00000504346.1:n.*1319C>T | |
| ENST00000677444.1:c.2042C>T | ||
| ENST00000677586.1:n.1464C>T | ||
| ENST00000677626.1:c.1746C>T | ENSP00000503552.1:p.Tyr582= | |
| ENST00000677853.1:c.*1105C>T | ENSP00000503488.1:n.*1105C>T | |
| ENST00000678264.1:c.*1474C>T | ENSP00000503157.1:n.*1474C>T | |
| ENST00000678303.1:c.2007C>T | ENSP00000503696.1:p.Tyr669= | |
| ENST00000678366.1:c.*2346C>T | ENSP00000504353.1:n.*2346C>T | |
| ENST00000678546.1:c.*2042C>T | ENSP00000503062.1:n.*2042C>T | |
| ENST00000678548.1:c.*2236C>T | ENSP00000503934.1:n.*2236C>T | |
| ENST00000678626.1:n.1933C>T | ||
| ENST00000678739.1:c.*2263C>T | ENSP00000503806.1:n.*2263C>T | |
| ENST00000678833.1:c.*1849C>T | ENSP00000503893.1:n.*1849C>T | |
| ENST00000679023.1:c.1935C>T | ENSP00000503718.1:p.Tyr645= | |
| ENST00000679076.1:c.1716C>T | ||
| ENST00000679111.1:c.*853C>T | ENSP00000504257.1:n.*853C>T | |
| ENST00000679189.1:c.1746C>T | ENSP00000503356.1:p.Tyr582= | |
| ENST00000341012.11:c.1935C>T | ENSP00000343034.7:p.Tyr645= | |
| ENST00000372220.4:c.960C>T | ENSP00000361294.4:p.Tyr320= | |
| ENST00000372228.7:c.2163C>T | ENSP00000361302.3:p.Tyr721= | |
| ENST00000402686.7:c.2097C>T | ENSP00000385797.3:p.Tyr699= | |
| ENST00000404875.6:c.1746C>T | ENSP00000384531.2:p.Tyr582= | |
| ENST00000423007.5:c.2097C>T | ENSP00000404119.1:p.Tyr699= | |
| ENST00000485278.5:n.2647C>T | ||
| NM_001077365.1:c.2097C>T | NP_001070833.1:p.Tyr699= | |
| NM_001077366.1:c.1935C>T | NP_001070834.1:p.Tyr645= | |
| NM_001136113.1:c.2097C>T | NP_001129585.1:p.Tyr699= | |
| NM_001136114.1:c.1746C>T | NP_001129586.1:p.Tyr582= | |
| NM_007171.3:c.2163C>T | NP_009102.3:p.Tyr721= | |
| XM_005272156.1:c.2163C>T | XP_005272213.1:p.Tyr721= | |
| XM_005272158.1:c.2001C>T | XP_005272215.1:p.Tyr667= | |
| XM_005272159.1:c.1812C>T | XP_005272216.1:p.Tyr604= | |
| XM_005272162.1:c.966C>T | XP_005272219.1:p.Tyr322= | |
| XM_006716932.1:c.1812C>T | XP_006716995.1:p.Tyr604= | |
| XM_011518140.1:c.2016C>T | XP_011516442.1:p.Tyr672= | |
| XM_011518141.1:c.1950C>T | XP_011516443.1:p.Tyr650= | |
| XM_011518142.1:c.1854C>T | XP_011516444.1:p.Tyr618= | |
| XM_011518143.1:c.1848C>T | XP_011516445.1:p.Tyr616= | |
| XM_011518145.1:c.1707C>T | XP_011516447.1:p.Tyr569= | |
| XM_011518147.1:c.1035C>T | XP_011516449.1:p.Tyr345= | |
| XR_929703.1:n.2339C>T | ||
| NM_001353193.1:c.2163C>T | NP_001340122.1:p.Tyr721= | |
| NM_001353194.1:c.1935C>T | NP_001340123.1:p.Tyr645= | |
| NM_001353195.1:c.1746C>T | NP_001340124.1:p.Tyr582= | |
| NM_001353196.1:c.2007C>T | NP_001340125.1:p.Tyr669= | |
| NM_001353197.1:c.2001C>T | NP_001340126.1:p.Tyr667= | |
| NM_001353198.1:c.2001C>T | NP_001340127.1:p.Tyr667= | |
| NM_001353199.1:c.1812C>T | NP_001340128.1:p.Tyr604= | |
| NM_001353200.1:c.1641C>T | NP_001340129.1:p.Tyr547= | |
| NR_148391.1:n.2147C>T | ||
| NR_148392.1:n.2365C>T | ||
| NR_148393.1:n.2286C>T | ||
| NR_148394.1:n.2040C>T | ||
| NR_148395.1:n.2438C>T | ||
| NR_148396.1:n.2072C>T | ||
| NR_148397.1:n.2197C>T | ||
| NR_148398.1:n.2152C>T | ||
| NR_148399.1:n.2678C>T | ||
| NR_148400.1:n.2277C>T | ||
| XM_005272162.3:c.966C>T | XP_005272219.1:p.Tyr322= | |
| XM_006716932.2:c.1812C>T | XP_006716995.1:p.Tyr604= | |
| XM_011518140.2:c.2016C>T | XP_011516442.1:p.Tyr672= | |
| XM_011518141.2:c.1950C>T | XP_011516443.1:p.Tyr650= | |
| XM_011518142.2:c.1854C>T | XP_011516444.1:p.Tyr618= | |
| XM_011518143.2:c.1848C>T | XP_011516445.1:p.Tyr616= | |
| XM_011518145.2:c.1707C>T | XP_011516447.1:p.Tyr569= | |
| XM_017014205.2:c.966C>T | XP_016869694.1:p.Tyr322= | |
| XM_024447380.1:c.966C>T | XP_024303148.1:p.Tyr322= | |
| XM_024447381.1:c.1272C>T | XP_024303149.1:p.Tyr424= | |
| XM_024447382.1:c.966C>T | XP_024303150.1:p.Tyr322= | |
| XR_001746160.2:n.2267C>T | ||
| XR_001746162.2:n.2472C>T | ||
| XR_001746164.1:n.2189C>T | ||
| XR_001746166.2:n.2484C>T | ||
| NM_001077365.2:c.2097C>T MANE Select | NP_001070833.1:p.Tyr699= | |
| NM_001077366.2:c.1935C>T | NP_001070834.1:p.Tyr645= | |
| NM_001136113.2:c.2097C>T | NP_001129585.1:p.Tyr699= | |
| NM_001136114.2:c.1746C>T | NP_001129586.1:p.Tyr582= | |
| NM_001353193.2:c.2163C>T | NP_001340122.2:p.Tyr721= | |
| NM_001353194.2:c.1935C>T | NP_001340123.1:p.Tyr645= | |
| NM_001353195.2:c.1746C>T | NP_001340124.1:p.Tyr582= | |
| NM_001353196.2:c.2007C>T | NP_001340125.1:p.Tyr669= | |
| NM_001353197.2:c.2001C>T | NP_001340126.2:p.Tyr667= | |
| NM_001353198.2:c.2001C>T | NP_001340127.2:p.Tyr667= | |
| NM_001353199.2:c.1812C>T | NP_001340128.2:p.Tyr604= | |
| NM_001353200.2:c.1641C>T | NP_001340129.1:p.Tyr547= | |
| NM_001374689.1:c.2085C>T | NP_001361618.1:p.Tyr695= | |
| NM_001374690.1:c.1878C>T | NP_001361619.1:p.Tyr626= | |
| NM_001374691.1:c.1746C>T | NP_001361620.1:p.Tyr582= | |
| NM_001374692.1:c.1746C>T | NP_001361621.1:p.Tyr582= | |
| NM_001374693.1:c.1746C>T | NP_001361622.1:p.Tyr582= | |
| NM_001374695.1:c.1707C>T | NP_001361624.1:p.Tyr569= | |
| NM_007171.4:c.2163C>T | NP_009102.4:p.Tyr721= | |
| NR_148391.2:n.2131C>T | ||
| NR_148392.2:n.2349C>T | ||
| NR_148393.2:n.2270C>T | ||
| NR_148394.2:n.2024C>T | ||
| NR_148395.2:n.2422C>T | ||
| NR_148396.2:n.2056C>T | ||
| NR_148397.2:n.2181C>T | ||
| NR_148398.2:n.2136C>T | ||
| NR_148399.2:n.2662C>T | ||
| NR_148400.2:n.2261C>T |