Linked Data
ClinVar Variation Id:
95458
dbSNP Id:
rs139687326
ExAC:
9:134394274 C / T
gnomAD v2:
9-134394274-C-T
gnomAD v3:
9-131518887-C-T
gnomAD v4:
9-131518887-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131518887C>T , CM000671.2:g.131518887C>T | GRCh38 |
| NC_000009.11:g.134394274C>T , CM000671.1:g.134394274C>T | GRCh37 |
| NC_000009.10:g.133384095C>T | NCBI36 |
| NG_008896.1:g.20986C>T | |
| NG_008896.2:g.20986C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.1254C>T | ENSP00000343034.7:p.Val418= | |
| ENST00000404875.7:n.1956C>T | ||
| ENST00000423007.6:c.1473C>T | ENSP00000404119.2:p.Val491= | |
| ENST00000677295.2:c.*1760C>T | ENSP00000504346.2:n.*1760C>T | |
| ENST00000678264.2:c.*1599C>T | ENSP00000503157.2:n.*1599C>T | |
| ENST00000682070.1:n.1881C>T | ||
| ENST00000682539.1:c.354C>T | ||
| ENST00000682813.1:n.1820C>T | ||
| ENST00000683392.1:n.4163C>T | ||
| ENST00000683712.1:n.1821C>T | ||
| ENST00000683900.1:n.3316C>T | ||
| ENST00000684062.1:n.2082C>T | ||
| ENST00000684579.1:n.3262C>T | ||
| ENST00000684679.1:n.643C>T | ||
| ENST00000341012.12:c.1254C>T | ENSP00000343034.7:p.Val418= | |
| ENST00000372220.5:c.285C>T | ENSP00000361294.5:p.Val95= | |
| ENST00000372228.9:c.1482C>T | ENSP00000361302.3:p.Val494= | |
| ENST00000402686.8:c.1416C>T MANE Select | ENSP00000385797.4:p.Val472= | |
| ENST00000676640.1:c.1416C>T | ENSP00000503281.1:p.Val472= | |
| ENST00000676803.1:c.591C>T | ENSP00000503093.1:p.Val197= | |
| ENST00000676835.1:c.*631C>T | ENSP00000502911.1:n.*631C>T | |
| ENST00000677029.1:c.960C>T | ENSP00000502936.1:p.Val320= | |
| ENST00000677099.1:c.*1126C>T | ENSP00000504553.1:n.*1126C>T | |
| ENST00000677216.1:c.1065C>T | ENSP00000503772.1:p.Val355= | |
| ENST00000677221.1:n.441C>T | ||
| ENST00000677295.1:c.*793C>T | ENSP00000504346.1:n.*793C>T | |
| ENST00000677444.1:c.1361C>T | ||
| ENST00000677586.1:n.897C>T | ||
| ENST00000677626.1:c.1065C>T | ENSP00000503552.1:p.Val355= | |
| ENST00000677677.1:n.1376C>T | ||
| ENST00000677853.1:c.*424C>T | ENSP00000503488.1:n.*424C>T | |
| ENST00000678202.1:n.575C>T | ||
| ENST00000678264.1:c.*793C>T | ENSP00000503157.1:n.*793C>T | |
| ENST00000678303.1:c.1326C>T | ENSP00000503696.1:p.Val442= | |
| ENST00000678366.1:c.*1665C>T | ENSP00000504353.1:n.*1665C>T | |
| ENST00000678546.1:c.*1361C>T | ENSP00000503062.1:n.*1361C>T | |
| ENST00000678548.1:c.*1488C>T | ENSP00000503934.1:n.*1488C>T | |
| ENST00000678626.1:n.1252C>T | ||
| ENST00000678733.1:c.497C>T | ||
| ENST00000678739.1:c.*1742C>T | ENSP00000503806.1:n.*1742C>T | |
| ENST00000678833.1:c.*863C>T | ENSP00000503893.1:n.*863C>T | |
| ENST00000679023.1:c.1254C>T | ENSP00000503718.1:p.Val418= | |
| ENST00000679076.1:c.1035C>T | ||
| ENST00000679111.1:c.*172C>T | ENSP00000504257.1:n.*172C>T | |
| ENST00000679189.1:c.1065C>T | ENSP00000503356.1:p.Val355= | |
| ENST00000341012.11:c.1254C>T | ENSP00000343034.7:p.Val418= | |
| ENST00000372220.4:c.279C>T | ENSP00000361294.4:p.Val93= | |
| ENST00000372228.7:c.1482C>T | ENSP00000361302.3:p.Val494= | |
| ENST00000402686.7:c.1416C>T | ENSP00000385797.3:p.Val472= | |
| ENST00000404875.6:c.1065C>T | ENSP00000384531.2:p.Val355= | |
| ENST00000423007.5:c.1416C>T | ENSP00000404119.1:p.Val472= | |
| ENST00000467848.1:n.120C>T | ||
| ENST00000485278.5:n.1971C>T | ||
| NM_001077365.1:c.1416C>T | NP_001070833.1:p.Val472= | |
| NM_001077366.1:c.1254C>T | NP_001070834.1:p.Val418= | |
| NM_001136113.1:c.1416C>T | NP_001129585.1:p.Val472= | |
| NM_001136114.1:c.1065C>T | NP_001129586.1:p.Val355= | |
| NM_007171.3:c.1482C>T | NP_009102.3:p.Val494= | |
| XM_005272156.1:c.1482C>T | XP_005272213.1:p.Val494= | |
| XM_005272158.1:c.1320C>T | XP_005272215.1:p.Val440= | |
| XM_005272159.1:c.1131C>T | XP_005272216.1:p.Val377= | |
| XM_005272162.1:c.285C>T | XP_005272219.1:p.Val95= | |
| XM_006716932.1:c.1131C>T | XP_006716995.1:p.Val377= | |
| XM_011518140.1:c.1335C>T | XP_011516442.1:p.Val445= | |
| XM_011518141.1:c.1269C>T | XP_011516443.1:p.Val423= | |
| XM_011518142.1:c.1173C>T | XP_011516444.1:p.Val391= | |
| XM_011518143.1:c.1167C>T | XP_011516445.1:p.Val389= | |
| XM_011518144.1:c.*172C>T | XP_011516446.1:n.*172C>T | |
| XM_011518145.1:c.1026C>T | XP_011516447.1:p.Val342= | |
| XM_011518146.1:c.*172C>T | XP_011516448.1:n.*172C>T | |
| XM_011518147.1:c.354C>T | XP_011516449.1:p.Val118= | |
| XR_929703.1:n.1658C>T | ||
| NM_001353193.1:c.1482C>T | NP_001340122.1:p.Val494= | |
| NM_001353194.1:c.1254C>T | NP_001340123.1:p.Val418= | |
| NM_001353195.1:c.1065C>T | NP_001340124.1:p.Val355= | |
| NM_001353196.1:c.1326C>T | NP_001340125.1:p.Val442= | |
| NM_001353197.1:c.1320C>T | NP_001340126.1:p.Val440= | |
| NM_001353198.1:c.1320C>T | NP_001340127.1:p.Val440= | |
| NM_001353199.1:c.1131C>T | NP_001340128.1:p.Val377= | |
| NM_001353200.1:c.960C>T | NP_001340129.1:p.Val320= | |
| NR_148391.1:n.1466C>T | ||
| NR_148392.1:n.1684C>T | ||
| NR_148393.1:n.1605C>T | ||
| NR_148394.1:n.1359C>T | ||
| NR_148395.1:n.1757C>T | ||
| NR_148396.1:n.1391C>T | ||
| NR_148397.1:n.1516C>T | ||
| NR_148398.1:n.1471C>T | ||
| NR_148399.1:n.1997C>T | ||
| NR_148400.1:n.1596C>T | ||
| XM_005272162.3:c.285C>T | XP_005272219.1:p.Val95= | |
| XM_006716932.2:c.1131C>T | XP_006716995.1:p.Val377= | |
| XM_011518140.2:c.1335C>T | XP_011516442.1:p.Val445= | |
| XM_011518141.2:c.1269C>T | XP_011516443.1:p.Val423= | |
| XM_011518142.2:c.1173C>T | XP_011516444.1:p.Val391= | |
| XM_011518143.2:c.1167C>T | XP_011516445.1:p.Val389= | |
| XM_011518145.2:c.1026C>T | XP_011516447.1:p.Val342= | |
| XM_017014205.2:c.285C>T | XP_016869694.1:p.Val95= | |
| XM_024447380.1:c.285C>T | XP_024303148.1:p.Val95= | |
| XM_024447381.1:c.591C>T | XP_024303149.1:p.Val197= | |
| XM_024447382.1:c.285C>T | XP_024303150.1:p.Val95= | |
| XR_001746160.2:n.1586C>T | ||
| XR_001746162.2:n.1791C>T | ||
| XR_001746164.1:n.1508C>T | ||
| XR_001746166.2:n.1803C>T | ||
| NM_001077365.2:c.1416C>T MANE Select | NP_001070833.1:p.Val472= | |
| NM_001077366.2:c.1254C>T | NP_001070834.1:p.Val418= | |
| NM_001136113.2:c.1416C>T | NP_001129585.1:p.Val472= | |
| NM_001136114.2:c.1065C>T | NP_001129586.1:p.Val355= | |
| NM_001353193.2:c.1482C>T | NP_001340122.2:p.Val494= | |
| NM_001353194.2:c.1254C>T | NP_001340123.1:p.Val418= | |
| NM_001353195.2:c.1065C>T | NP_001340124.1:p.Val355= | |
| NM_001353196.2:c.1326C>T | NP_001340125.1:p.Val442= | |
| NM_001353197.2:c.1320C>T | NP_001340126.2:p.Val440= | |
| NM_001353198.2:c.1320C>T | NP_001340127.2:p.Val440= | |
| NM_001353199.2:c.1131C>T | NP_001340128.2:p.Val377= | |
| NM_001353200.2:c.960C>T | NP_001340129.1:p.Val320= | |
| NM_001374689.1:c.1404C>T | NP_001361618.1:p.Val468= | |
| NM_001374690.1:c.1365+350C>T | NP_001361619.1:n.1365+350C>T | |
| NM_001374691.1:c.1065C>T | NP_001361620.1:p.Val355= | |
| NM_001374692.1:c.1065C>T | NP_001361621.1:p.Val355= | |
| NM_001374693.1:c.1065C>T | NP_001361622.1:p.Val355= | |
| NM_001374695.1:c.1026C>T | NP_001361624.1:p.Val342= | |
| NM_007171.4:c.1482C>T | NP_009102.4:p.Val494= | |
| NR_148391.2:n.1450C>T | ||
| NR_148392.2:n.1668C>T | ||
| NR_148393.2:n.1589C>T | ||
| NR_148394.2:n.1343C>T | ||
| NR_148395.2:n.1741C>T | ||
| NR_148396.2:n.1375C>T | ||
| NR_148397.2:n.1500C>T | ||
| NR_148398.2:n.1455C>T | ||
| NR_148399.2:n.1981C>T | ||
| NR_148400.2:n.1580C>T |