Linked Data
ClinVar Variation Id:
289444
dbSNP Id:
rs547775333
ExAC:
9:134394353 G / A
gnomAD v2:
9-134394353-G-A
gnomAD v3:
9-131518966-G-A
gnomAD v4:
9-131518966-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131518966G>A , CM000671.2:g.131518966G>A | GRCh38 |
| NC_000009.11:g.134394353G>A , CM000671.1:g.134394353G>A | GRCh37 |
| NC_000009.10:g.133384174G>A | NCBI36 |
| NG_008896.1:g.21065G>A | |
| NG_008896.2:g.21065G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.1324+9G>A | ENSP00000343034.7:n.1324+9G>A | |
| ENST00000404875.7:n.2026+9G>A | ||
| ENST00000423007.6:c.1543+9G>A | ENSP00000404119.2:n.1543+9G>A | |
| ENST00000677295.2:c.*1830+9G>A | ENSP00000504346.2:n.*1830+9G>A | |
| ENST00000678264.2:c.*1669+9G>A | ENSP00000503157.2:n.*1669+9G>A | |
| ENST00000682070.1:n.1951+9G>A | ||
| ENST00000682813.1:n.1890+9G>A | ||
| ENST00000683392.1:n.4233+9G>A | ||
| ENST00000683712.1:n.1891+9G>A | ||
| ENST00000683900.1:n.3386+9G>A | ||
| ENST00000684062.1:n.2152+9G>A | ||
| ENST00000684579.1:n.3332+9G>A | ||
| ENST00000684679.1:n.713+9G>A | ||
| ENST00000341012.12:c.1324+9G>A | ENSP00000343034.7:n.1324+9G>A | |
| ENST00000372220.5:c.355+9G>A | ENSP00000361294.5:n.355+9G>A | |
| ENST00000372228.9:c.1552+9G>A | ENSP00000361302.3:n.1552+9G>A | |
| ENST00000402686.8:c.1486+9G>A MANE Select | ENSP00000385797.4:n.1486+9G>A | |
| ENST00000676640.1:c.1486+9G>A | ENSP00000503281.1:n.1486+9G>A | |
| ENST00000676803.1:c.661+9G>A | ENSP00000503093.1:n.661+9G>A | |
| ENST00000676835.1:c.*701+9G>A | ENSP00000502911.1:n.*701+9G>A | |
| ENST00000677029.1:c.1030+9G>A | ENSP00000502936.1:n.1030+9G>A | |
| ENST00000677099.1:c.*1196+9G>A | ENSP00000504553.1:n.*1196+9G>A | |
| ENST00000677216.1:c.1135+9G>A | ENSP00000503772.1:n.1135+9G>A | |
| ENST00000677221.1:n.511+9G>A | ||
| ENST00000677295.1:c.*863+9G>A | ENSP00000504346.1:n.*863+9G>A | |
| ENST00000677444.1:c.1431+9G>A | ||
| ENST00000677586.1:n.967+9G>A | ||
| ENST00000677626.1:c.1135+9G>A | ENSP00000503552.1:n.1135+9G>A | |
| ENST00000677677.1:n.1446+9G>A | ||
| ENST00000677853.1:c.*494+9G>A | ENSP00000503488.1:n.*494+9G>A | |
| ENST00000678202.1:n.645+9G>A | ||
| ENST00000678264.1:c.*863+9G>A | ENSP00000503157.1:n.*863+9G>A | |
| ENST00000678303.1:c.1396+9G>A | ENSP00000503696.1:n.1396+9G>A | |
| ENST00000678366.1:c.*1735+9G>A | ENSP00000504353.1:n.*1735+9G>A | |
| ENST00000678546.1:c.*1431+9G>A | ENSP00000503062.1:n.*1431+9G>A | |
| ENST00000678548.1:c.*1558+9G>A | ENSP00000503934.1:n.*1558+9G>A | |
| ENST00000678626.1:n.1322+9G>A | ||
| ENST00000678733.1:c.567+9G>A | ||
| ENST00000678739.1:c.*1812+9G>A | ENSP00000503806.1:n.*1812+9G>A | |
| ENST00000678833.1:c.*933+9G>A | ENSP00000503893.1:n.*933+9G>A | |
| ENST00000679023.1:c.1324+9G>A | ENSP00000503718.1:n.1324+9G>A | |
| ENST00000679076.1:c.1105+9G>A | ||
| ENST00000679111.1:c.*242+9G>A | ENSP00000504257.1:n.*242+9G>A | |
| ENST00000679189.1:c.1135+9G>A | ENSP00000503356.1:n.1135+9G>A | |
| ENST00000341012.11:c.1324+9G>A | ENSP00000343034.7:n.1324+9G>A | |
| ENST00000372220.4:c.349+9G>A | ENSP00000361294.4:n.349+9G>A | |
| ENST00000372228.7:c.1552+9G>A | ENSP00000361302.3:n.1552+9G>A | |
| ENST00000402686.7:c.1486+9G>A | ENSP00000385797.3:n.1486+9G>A | |
| ENST00000404875.6:c.1135+9G>A | ENSP00000384531.2:n.1135+9G>A | |
| ENST00000423007.5:c.1486+9G>A | ENSP00000404119.1:n.1486+9G>A | |
| ENST00000467848.1:n.190+9G>A | ||
| ENST00000485278.5:n.2041+9G>A | ||
| NM_001077365.1:c.1486+9G>A | NP_001070833.1:n.1486+9G>A | |
| NM_001077366.1:c.1324+9G>A | NP_001070834.1:n.1324+9G>A | |
| NM_001136113.1:c.1486+9G>A | NP_001129585.1:n.1486+9G>A | |
| NM_001136114.1:c.1135+9G>A | NP_001129586.1:n.1135+9G>A | |
| NM_007171.3:c.1552+9G>A | NP_009102.3:n.1552+9G>A | |
| XM_005272156.1:c.1552+9G>A | XP_005272213.1:n.1552+9G>A | |
| XM_005272158.1:c.1390+9G>A | XP_005272215.1:n.1390+9G>A | |
| XM_005272159.1:c.1201+9G>A | XP_005272216.1:n.1201+9G>A | |
| XM_005272162.1:c.355+9G>A | XP_005272219.1:n.355+9G>A | |
| XM_006716932.1:c.1201+9G>A | XP_006716995.1:n.1201+9G>A | |
| XM_011518140.1:c.1405+9G>A | XP_011516442.1:n.1405+9G>A | |
| XM_011518141.1:c.1339+9G>A | XP_011516443.1:n.1339+9G>A | |
| XM_011518142.1:c.1243+9G>A | XP_011516444.1:n.1243+9G>A | |
| XM_011518143.1:c.1237+9G>A | XP_011516445.1:n.1237+9G>A | |
| XM_011518145.1:c.1096+9G>A | XP_011516447.1:n.1096+9G>A | |
| XM_011518147.1:c.424+9G>A | XP_011516449.1:n.424+9G>A | |
| XR_929703.1:n.1728+9G>A | ||
| NM_001353193.1:c.1552+9G>A | NP_001340122.1:n.1552+9G>A | |
| NM_001353194.1:c.1324+9G>A | NP_001340123.1:n.1324+9G>A | |
| NM_001353195.1:c.1135+9G>A | NP_001340124.1:n.1135+9G>A | |
| NM_001353196.1:c.1396+9G>A | NP_001340125.1:n.1396+9G>A | |
| NM_001353197.1:c.1390+9G>A | NP_001340126.1:n.1390+9G>A | |
| NM_001353198.1:c.1390+9G>A | NP_001340127.1:n.1390+9G>A | |
| NM_001353199.1:c.1201+9G>A | NP_001340128.1:n.1201+9G>A | |
| NM_001353200.1:c.1030+9G>A | NP_001340129.1:n.1030+9G>A | |
| NR_148391.1:n.1536+9G>A | ||
| NR_148392.1:n.1754+9G>A | ||
| NR_148393.1:n.1675+9G>A | ||
| NR_148394.1:n.1429+9G>A | ||
| NR_148395.1:n.1827+9G>A | ||
| NR_148396.1:n.1461+9G>A | ||
| NR_148397.1:n.1586+9G>A | ||
| NR_148398.1:n.1541+9G>A | ||
| NR_148399.1:n.2067+9G>A | ||
| NR_148400.1:n.1666+9G>A | ||
| XM_005272162.3:c.355+9G>A | XP_005272219.1:n.355+9G>A | |
| XM_006716932.2:c.1201+9G>A | XP_006716995.1:n.1201+9G>A | |
| XM_011518140.2:c.1405+9G>A | XP_011516442.1:n.1405+9G>A | |
| XM_011518141.2:c.1339+9G>A | XP_011516443.1:n.1339+9G>A | |
| XM_011518142.2:c.1243+9G>A | XP_011516444.1:n.1243+9G>A | |
| XM_011518143.2:c.1237+9G>A | XP_011516445.1:n.1237+9G>A | |
| XM_011518145.2:c.1096+9G>A | XP_011516447.1:n.1096+9G>A | |
| XM_017014205.2:c.355+9G>A | XP_016869694.1:n.355+9G>A | |
| XM_024447380.1:c.355+9G>A | XP_024303148.1:n.355+9G>A | |
| XM_024447381.1:c.661+9G>A | XP_024303149.1:n.661+9G>A | |
| XM_024447382.1:c.355+9G>A | XP_024303150.1:n.355+9G>A | |
| XR_001746160.2:n.1656+9G>A | ||
| XR_001746162.2:n.1861+9G>A | ||
| XR_001746164.1:n.1578+9G>A | ||
| XR_001746166.2:n.1873+9G>A | ||
| NM_001077365.2:c.1486+9G>A MANE Select | NP_001070833.1:n.1486+9G>A | |
| NM_001077366.2:c.1324+9G>A | NP_001070834.1:n.1324+9G>A | |
| NM_001136113.2:c.1486+9G>A | NP_001129585.1:n.1486+9G>A | |
| NM_001136114.2:c.1135+9G>A | NP_001129586.1:n.1135+9G>A | |
| NM_001353193.2:c.1552+9G>A | NP_001340122.2:n.1552+9G>A | |
| NM_001353194.2:c.1324+9G>A | NP_001340123.1:n.1324+9G>A | |
| NM_001353195.2:c.1135+9G>A | NP_001340124.1:n.1135+9G>A | |
| NM_001353196.2:c.1396+9G>A | NP_001340125.1:n.1396+9G>A | |
| NM_001353197.2:c.1390+9G>A | NP_001340126.2:n.1390+9G>A | |
| NM_001353198.2:c.1390+9G>A | NP_001340127.2:n.1390+9G>A | |
| NM_001353199.2:c.1201+9G>A | NP_001340128.2:n.1201+9G>A | |
| NM_001353200.2:c.1030+9G>A | NP_001340129.1:n.1030+9G>A | |
| NM_001374689.1:c.1474+9G>A | NP_001361618.1:n.1474+9G>A | |
| NM_001374690.1:c.1365+429G>A | NP_001361619.1:n.1365+429G>A | |
| NM_001374691.1:c.1135+9G>A | NP_001361620.1:n.1135+9G>A | |
| NM_001374692.1:c.1135+9G>A | NP_001361621.1:n.1135+9G>A | |
| NM_001374693.1:c.1135+9G>A | NP_001361622.1:n.1135+9G>A | |
| NM_001374695.1:c.1096+9G>A | NP_001361624.1:n.1096+9G>A | |
| NM_007171.4:c.1552+9G>A | NP_009102.4:n.1552+9G>A | |
| NR_148391.2:n.1520+9G>A | ||
| NR_148392.2:n.1738+9G>A | ||
| NR_148393.2:n.1659+9G>A | ||
| NR_148394.2:n.1413+9G>A | ||
| NR_148395.2:n.1811+9G>A | ||
| NR_148396.2:n.1445+9G>A | ||
| NR_148397.2:n.1570+9G>A | ||
| NR_148398.2:n.1525+9G>A | ||
| NR_148399.2:n.2051+9G>A | ||
| NR_148400.2:n.1650+9G>A |