Linked Data
ClinVar Variation Id:
538728
dbSNP Id:
rs753694905
gnomAD v2:
9-134386795-C-T
gnomAD v4:
9-131511408-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131511408C>T , CM000671.2:g.131511408C>T | GRCh38 |
| NC_000009.11:g.134386795C>T , CM000671.1:g.134386795C>T | GRCh37 |
| NC_000009.10:g.133376616C>T | NCBI36 |
| NG_008896.1:g.13507C>T | |
| NG_008896.2:g.13507C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.765C>T | ENSP00000343034.7:p.Asn255= | |
| ENST00000404875.7:n.1299C>T | ||
| ENST00000423007.6:c.984C>T | ENSP00000404119.2:p.Asn328= | |
| ENST00000677295.2:c.*1266C>T | ENSP00000504346.2:n.*1266C>T | |
| ENST00000678264.2:c.*1110C>T | ENSP00000503157.2:n.*1110C>T | |
| ENST00000678942.2:c.*480C>T | ENSP00000504690.2:n.*480C>T | |
| ENST00000682070.1:n.1387C>T | ||
| ENST00000682813.1:n.1192C>T | ||
| ENST00000683134.1:c.294C>T | ||
| ENST00000683392.1:n.3674C>T | ||
| ENST00000683712.1:n.1327C>T | ||
| ENST00000683900.1:n.2254C>T | ||
| ENST00000684062.1:n.1593C>T | ||
| ENST00000684579.1:n.2768C>T | ||
| ENST00000341012.12:c.765C>T | ENSP00000343034.7:p.Asn255= | |
| ENST00000372220.5:c.-145-633C>T | ENSP00000361294.5:n.-145-633C>T | |
| ENST00000372228.9:c.993C>T | ENSP00000361302.3:p.Asn331= | |
| ENST00000402686.8:c.927C>T MANE Select | ENSP00000385797.4:p.Asn309= | |
| ENST00000415075.6:c.*380C>T | ENSP00000405149.2:n.*380C>T | |
| ENST00000676640.1:c.927C>T | ENSP00000503281.1:p.Asn309= | |
| ENST00000676803.1:c.102C>T | ENSP00000503093.1:p.Asn34= | |
| ENST00000676835.1:c.*137C>T | ENSP00000502911.1:n.*137C>T | |
| ENST00000677029.1:c.471C>T | ENSP00000502936.1:p.Asn157= | |
| ENST00000677099.1:c.*637C>T | ENSP00000504553.1:n.*637C>T | |
| ENST00000677216.1:c.576C>T | ENSP00000503772.1:p.Asn192= | |
| ENST00000677293.1:c.102C>T | ENSP00000504278.1:p.Asn34= | |
| ENST00000677295.1:c.*299C>T | ENSP00000504346.1:n.*299C>T | |
| ENST00000677444.1:c.733C>T | ||
| ENST00000677586.1:n.408C>T | ||
| ENST00000677626.1:c.765C>T | ENSP00000503552.1:p.Asn255= | |
| ENST00000677677.1:n.887C>T | ||
| ENST00000677853.1:c.508C>T | ENSP00000503488.1:p.Arg170Cys | |
| ENST00000677944.1:c.189C>T | ||
| ENST00000678264.1:c.*299C>T | ENSP00000503157.1:n.*299C>T | |
| ENST00000678303.1:c.837C>T | ENSP00000503696.1:p.Asn279= | |
| ENST00000678366.1:c.*1176C>T | ENSP00000504353.1:n.*1176C>T | |
| ENST00000678546.1:c.*299C>T | ENSP00000503062.1:n.*299C>T | |
| ENST00000678548.1:c.*994C>T | ENSP00000503934.1:n.*994C>T | |
| ENST00000678626.1:n.619C>T | ||
| ENST00000678733.1:c.101C>T | ||
| ENST00000678739.1:c.*1248C>T | ENSP00000503806.1:n.*1248C>T | |
| ENST00000678833.1:c.*374C>T | ENSP00000503893.1:n.*374C>T | |
| ENST00000678942.1:c.102C>T | ENSP00000504690.1:p.Asn34= | |
| ENST00000679023.1:c.765C>T | ENSP00000503718.1:p.Asn255= | |
| ENST00000679073.1:c.305C>T | ENSP00000504356.1:n.305C>T | |
| ENST00000679076.1:c.541C>T | ||
| ENST00000679111.1:c.927C>T | ENSP00000504257.1:p.Asn309= | |
| ENST00000679189.1:c.576C>T | ENSP00000503356.1:p.Asn192= | |
| ENST00000341012.11:c.765C>T | ENSP00000343034.7:p.Asn255= | |
| ENST00000372228.7:c.993C>T | ENSP00000361302.3:p.Asn331= | |
| ENST00000402686.7:c.927C>T | ENSP00000385797.3:p.Asn309= | |
| ENST00000404875.6:c.576C>T | ENSP00000384531.2:p.Asn192= | |
| ENST00000415075.5:c.319C>T | ENSP00000405149.1:p.Arg107Cys | |
| ENST00000423007.5:c.927C>T | ENSP00000404119.1:p.Asn309= | |
| ENST00000441334.5:c.642C>T | ENSP00000395060.1:p.Asn214= | |
| ENST00000462375.5:n.748C>T | ||
| ENST00000485278.5:n.909C>T | ||
| NM_001077365.1:c.927C>T | NP_001070833.1:p.Asn309= | |
| NM_001077366.1:c.765C>T | NP_001070834.1:p.Asn255= | |
| NM_001136113.1:c.927C>T | NP_001129585.1:p.Asn309= | |
| NM_001136114.1:c.576C>T | NP_001129586.1:p.Asn192= | |
| NM_007171.3:c.993C>T | NP_009102.3:p.Asn331= | |
| XM_005272156.1:c.993C>T | XP_005272213.1:p.Asn331= | |
| XM_005272158.1:c.831C>T | XP_005272215.1:p.Asn277= | |
| XM_005272159.1:c.642C>T | XP_005272216.1:p.Asn214= | |
| XM_005272162.1:c.-210C>T | XP_005272219.1:n.-210C>T | |
| XM_006716932.1:c.642C>T | XP_006716995.1:p.Asn214= | |
| XM_011518140.1:c.846C>T | XP_011516442.1:p.Asn282= | |
| XM_011518141.1:c.780C>T | XP_011516443.1:p.Asn260= | |
| XM_011518142.1:c.684C>T | XP_011516444.1:p.Asn228= | |
| XM_011518143.1:c.673C>T | XP_011516445.1:p.Arg225Cys | |
| XM_011518144.1:c.993C>T | XP_011516446.1:p.Asn331= | |
| XM_011518145.1:c.537C>T | XP_011516447.1:p.Asn179= | |
| XM_011518146.1:c.673C>T | XP_011516448.1:p.Arg225Cys | |
| XR_929703.1:n.1169C>T | ||
| NM_001353193.1:c.993C>T | NP_001340122.1:p.Asn331= | |
| NM_001353194.1:c.765C>T | NP_001340123.1:p.Asn255= | |
| NM_001353195.1:c.576C>T | NP_001340124.1:p.Asn192= | |
| NM_001353196.1:c.837C>T | NP_001340125.1:p.Asn279= | |
| NM_001353197.1:c.831C>T | NP_001340126.1:p.Asn277= | |
| NM_001353198.1:c.831C>T | NP_001340127.1:p.Asn277= | |
| NM_001353199.1:c.642C>T | NP_001340128.1:p.Asn214= | |
| NM_001353200.1:c.471C>T | NP_001340129.1:p.Asn157= | |
| NR_148391.1:n.977C>T | ||
| NR_148392.1:n.1195C>T | ||
| NR_148393.1:n.977C>T | ||
| NR_148394.1:n.865C>T | ||
| NR_148395.1:n.1129C>T | ||
| NR_148396.1:n.758C>T | ||
| NR_148397.1:n.1022C>T | ||
| NR_148398.1:n.977C>T | ||
| NR_148399.1:n.1369C>T | ||
| NR_148400.1:n.963C>T | ||
| XM_005272162.3:c.-210C>T | XP_005272219.1:n.-210C>T | |
| XM_006716932.2:c.642C>T | XP_006716995.1:p.Asn214= | |
| XM_011518140.2:c.846C>T | XP_011516442.1:p.Asn282= | |
| XM_011518141.2:c.780C>T | XP_011516443.1:p.Asn260= | |
| XM_011518142.2:c.684C>T | XP_011516444.1:p.Asn228= | |
| XM_011518143.2:c.673C>T | XP_011516445.1:p.Arg225Cys | |
| XM_011518145.2:c.537C>T | XP_011516447.1:p.Asn179= | |
| XM_017014205.2:c.-210C>T | XP_016869694.1:n.-210C>T | |
| XM_024447380.1:c.-210C>T | XP_024303148.1:n.-210C>T | |
| XM_024447381.1:c.102C>T | XP_024303149.1:p.Asn34= | |
| XM_024447382.1:c.-210C>T | XP_024303150.1:n.-210C>T | |
| XR_001746160.2:n.1097C>T | ||
| XR_001746162.2:n.1163C>T | ||
| XR_001746164.1:n.875C>T | ||
| XR_001746166.2:n.1314C>T | ||
| NM_001077365.2:c.927C>T MANE Select | NP_001070833.1:p.Asn309= | |
| NM_001077366.2:c.765C>T | NP_001070834.1:p.Asn255= | |
| NM_001136113.2:c.927C>T | NP_001129585.1:p.Asn309= | |
| NM_001136114.2:c.576C>T | NP_001129586.1:p.Asn192= | |
| NM_001353193.2:c.993C>T | NP_001340122.2:p.Asn331= | |
| NM_001353194.2:c.765C>T | NP_001340123.1:p.Asn255= | |
| NM_001353195.2:c.576C>T | NP_001340124.1:p.Asn192= | |
| NM_001353196.2:c.837C>T | NP_001340125.1:p.Asn279= | |
| NM_001353197.2:c.831C>T | NP_001340126.2:p.Asn277= | |
| NM_001353198.2:c.831C>T | NP_001340127.2:p.Asn277= | |
| NM_001353199.2:c.642C>T | NP_001340128.2:p.Asn214= | |
| NM_001353200.2:c.471C>T | NP_001340129.1:p.Asn157= | |
| NM_001374689.1:c.910C>T | NP_001361618.1:p.Arg304Cys | |
| NM_001374690.1:c.927C>T | NP_001361619.1:p.Asn309= | |
| NM_001374691.1:c.576C>T | NP_001361620.1:p.Asn192= | |
| NM_001374692.1:c.576C>T | NP_001361621.1:p.Asn192= | |
| NM_001374693.1:c.765C>T | NP_001361622.1:p.Asn255= | |
| NM_001374695.1:c.537C>T | NP_001361624.1:p.Asn179= | |
| NM_007171.4:c.993C>T | NP_009102.4:p.Asn331= | |
| NR_148391.2:n.961C>T | ||
| NR_148392.2:n.1179C>T | ||
| NR_148393.2:n.961C>T | ||
| NR_148394.2:n.849C>T | ||
| NR_148395.2:n.1113C>T | ||
| NR_148396.2:n.742C>T | ||
| NR_148397.2:n.1006C>T | ||
| NR_148398.2:n.961C>T | ||
| NR_148399.2:n.1353C>T | ||
| NR_148400.2:n.947C>T |