Linked Data
ClinVar Variation Id:
2924691
ClinVar RCV Id:
RCV003788393
dbSNP Id:
rs767287237
gnomAD v4:
9-131509812-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131509812A>G , CM000671.2:g.131509812A>G | GRCh38 |
| NC_000009.11:g.134385199A>G , CM000671.1:g.134385199A>G | GRCh37 |
| NC_000009.10:g.133375020A>G | NCBI36 |
| NG_008896.1:g.11911A>G | |
| NG_008896.2:g.11911A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.443+4A>G | ENSP00000343034.7:n.443+4A>G | |
| ENST00000404875.7:n.714+4A>G | ||
| ENST00000423007.6:c.596+4A>G | ENSP00000404119.2:n.596+4A>G | |
| ENST00000462375.7:n.113-91A>G | ||
| ENST00000677295.2:c.*681+4A>G | ENSP00000504346.2:n.*681+4A>G | |
| ENST00000678264.2:c.*788+4A>G | ENSP00000503157.2:n.*788+4A>G | |
| ENST00000678942.2:c.300+4A>G | ENSP00000504690.2:n.300+4A>G | |
| ENST00000682070.1:n.802+4A>G | ||
| ENST00000682813.1:n.607+4A>G | ||
| ENST00000683134.1:c.66+4A>G | ||
| ENST00000683392.1:n.3089+4A>G | ||
| ENST00000683712.1:n.742+4A>G | ||
| ENST00000683900.1:n.1669+4A>G | ||
| ENST00000684062.1:n.918A>G | ||
| ENST00000684579.1:n.2183+4A>G | ||
| ENST00000341012.12:c.443+4A>G | ENSP00000343034.7:n.443+4A>G | |
| ENST00000372220.5:c.-145-2229A>G | ENSP00000361294.5:n.-145-2229A>G | |
| ENST00000372228.9:c.605+4A>G | ENSP00000361302.3:n.605+4A>G | |
| ENST00000402686.8:c.605+4A>G MANE Select | ENSP00000385797.4:n.605+4A>G | |
| ENST00000415075.6:c.*250-545A>G | ENSP00000405149.2:n.*250-545A>G | |
| ENST00000430619.2:c.149+4A>G | ENSP00000402083.2:n.149+4A>G | |
| ENST00000462375.6:n.429+4A>G | ||
| ENST00000676640.1:c.605+4A>G | ENSP00000503281.1:n.605+4A>G | |
| ENST00000676803.1:c.-126-448A>G | ENSP00000503093.1:n.-126-448A>G | |
| ENST00000676835.1:c.189-448A>G | ENSP00000502911.1:n.189-448A>G | |
| ENST00000676915.1:c.458+4A>G | ENSP00000504628.1:n.458+4A>G | |
| ENST00000677028.1:c.*52+4A>G | ENSP00000503896.1:n.*52+4A>G | |
| ENST00000677029.1:c.149+4A>G | ENSP00000502936.1:n.149+4A>G | |
| ENST00000677099.1:c.*315+4A>G | ENSP00000504553.1:n.*315+4A>G | |
| ENST00000677216.1:c.254+4A>G | ENSP00000503772.1:n.254+4A>G | |
| ENST00000677293.1:c.-29-545A>G | ENSP00000504278.1:n.-29-545A>G | |
| ENST00000677295.1:c.443+4A>G | ENSP00000504346.1:n.443+4A>G | |
| ENST00000677444.1:c.148+4A>G | ||
| ENST00000677586.1:n.181-448A>G | ||
| ENST00000677626.1:c.443+4A>G | ENSP00000503552.1:n.443+4A>G | |
| ENST00000677677.1:n.565+4A>G | ||
| ENST00000677729.1:c.*52+4A>G | ENSP00000503581.1:n.*52+4A>G | |
| ENST00000677853.1:c.378-545A>G | ENSP00000503488.1:n.378-545A>G | |
| ENST00000677944.1:c.59-545A>G | ||
| ENST00000678264.1:c.605+4A>G | ENSP00000503157.1:n.605+4A>G | |
| ENST00000678303.1:c.515+4A>G | ENSP00000503696.1:n.515+4A>G | |
| ENST00000678366.1:c.*788+4A>G | ENSP00000504353.1:n.*788+4A>G | |
| ENST00000678546.1:c.443+4A>G | ENSP00000503062.1:n.443+4A>G | |
| ENST00000678548.1:c.*319A>G | ENSP00000503934.1:n.*319A>G | |
| ENST00000678626.1:n.297+4A>G | ||
| ENST00000678693.1:n.288+4A>G | ||
| ENST00000678707.1:n.243+4A>G | ||
| ENST00000678739.1:c.*663+4A>G | ENSP00000503806.1:n.*663+4A>G | |
| ENST00000678833.1:c.*52+4A>G | ENSP00000503893.1:n.*52+4A>G | |
| ENST00000679023.1:c.443+4A>G | ENSP00000503718.1:n.443+4A>G | |
| ENST00000679076.1:c.316+4A>G | ||
| ENST00000679111.1:c.605+4A>G | ENSP00000504257.1:n.605+4A>G | |
| ENST00000679189.1:c.254+4A>G | ENSP00000503356.1:n.254+4A>G | |
| ENST00000341012.11:c.443+4A>G | ENSP00000343034.7:n.443+4A>G | |
| ENST00000372228.7:c.605+4A>G | ENSP00000361302.3:n.605+4A>G | |
| ENST00000402686.7:c.605+4A>G | ENSP00000385797.3:n.605+4A>G | |
| ENST00000404875.6:c.254+4A>G | ENSP00000384531.2:n.254+4A>G | |
| ENST00000415075.5:c.189-545A>G | ENSP00000405149.1:n.189-545A>G | |
| ENST00000423007.5:c.605+4A>G | ENSP00000404119.1:n.605+4A>G | |
| ENST00000430619.1:c.254+4A>G | ENSP00000402083.1:n.254+4A>G | |
| ENST00000441334.5:c.254+4A>G | ENSP00000395060.1:n.254+4A>G | |
| ENST00000448212.5:c.443+4A>G | ENSP00000403736.1:n.443+4A>G | |
| ENST00000462375.5:n.163+4A>G | ||
| NM_001077365.1:c.605+4A>G | NP_001070833.1:n.605+4A>G | |
| NM_001077366.1:c.443+4A>G | NP_001070834.1:n.443+4A>G | |
| NM_001136113.1:c.605+4A>G | NP_001129585.1:n.605+4A>G | |
| NM_001136114.1:c.254+4A>G | NP_001129586.1:n.254+4A>G | |
| NM_007171.3:c.605+4A>G | NP_009102.3:n.605+4A>G | |
| XM_005272156.1:c.605+4A>G | XP_005272213.1:n.605+4A>G | |
| XM_005272158.1:c.443+4A>G | XP_005272215.1:n.443+4A>G | |
| XM_005272159.1:c.254+4A>G | XP_005272216.1:n.254+4A>G | |
| XM_005272162.1:c.-795+4A>G | XP_005272219.1:n.-795+4A>G | |
| XM_006716932.1:c.254+4A>G | XP_006716995.1:n.254+4A>G | |
| XM_011518140.1:c.458+4A>G | XP_011516442.1:n.458+4A>G | |
| XM_011518141.1:c.458+4A>G | XP_011516443.1:n.458+4A>G | |
| XM_011518142.1:c.296+4A>G | XP_011516444.1:n.296+4A>G | |
| XM_011518143.1:c.351+4A>G | XP_011516445.1:n.351+4A>G | |
| XM_011518144.1:c.605+4A>G | XP_011516446.1:n.605+4A>G | |
| XM_011518145.1:c.149+4A>G | XP_011516447.1:n.149+4A>G | |
| XM_011518146.1:c.351+4A>G | XP_011516448.1:n.351+4A>G | |
| XR_929703.1:n.781+4A>G | ||
| NM_001353193.1:c.605+4A>G | NP_001340122.1:n.605+4A>G | |
| NM_001353194.1:c.443+4A>G | NP_001340123.1:n.443+4A>G | |
| NM_001353195.1:c.254+4A>G | NP_001340124.1:n.254+4A>G | |
| NM_001353196.1:c.515+4A>G | NP_001340125.1:n.515+4A>G | |
| NM_001353197.1:c.443+4A>G | NP_001340126.1:n.443+4A>G | |
| NM_001353198.1:c.443+4A>G | NP_001340127.1:n.443+4A>G | |
| NM_001353199.1:c.254+4A>G | NP_001340128.1:n.254+4A>G | |
| NM_001353200.1:c.149+4A>G | NP_001340129.1:n.149+4A>G | |
| NR_148391.1:n.655+4A>G | ||
| NR_148392.1:n.807+4A>G | ||
| NR_148393.1:n.655+4A>G | ||
| NR_148394.1:n.543+4A>G | ||
| NR_148395.1:n.807+4A>G | ||
| NR_148396.1:n.436+4A>G | ||
| NR_148397.1:n.700+4A>G | ||
| NR_148398.1:n.655+4A>G | ||
| NR_148399.1:n.1047+4A>G | ||
| NR_148400.1:n.641+4A>G | ||
| XM_005272162.3:c.-795+4A>G | XP_005272219.1:n.-795+4A>G | |
| XM_006716932.2:c.254+4A>G | XP_006716995.1:n.254+4A>G | |
| XM_011518140.2:c.458+4A>G | XP_011516442.1:n.458+4A>G | |
| XM_011518141.2:c.458+4A>G | XP_011516443.1:n.458+4A>G | |
| XM_011518142.2:c.296+4A>G | XP_011516444.1:n.296+4A>G | |
| XM_011518143.2:c.351+4A>G | XP_011516445.1:n.351+4A>G | |
| XM_011518145.2:c.149+4A>G | XP_011516447.1:n.149+4A>G | |
| XM_017014205.2:c.-598+4A>G | XP_016869694.1:n.-598+4A>G | |
| XM_024447380.1:c.-532+4A>G | XP_024303148.1:n.-532+4A>G | |
| XM_024447381.1:c.-484+4A>G | XP_024303149.1:n.-484+4A>G | |
| XM_024447382.1:c.-795+4A>G | XP_024303150.1:n.-795+4A>G | |
| XR_001746160.2:n.775+4A>G | ||
| XR_001746162.2:n.775+4A>G | ||
| XR_001746164.1:n.553+4A>G | ||
| XR_001746166.2:n.729+4A>G | ||
| NM_001077365.2:c.605+4A>G MANE Select | NP_001070833.1:n.605+4A>G | |
| NM_001077366.2:c.443+4A>G | NP_001070834.1:n.443+4A>G | |
| NM_001136113.2:c.605+4A>G | NP_001129585.1:n.605+4A>G | |
| NM_001136114.2:c.254+4A>G | NP_001129586.1:n.254+4A>G | |
| NM_001353193.2:c.605+4A>G | NP_001340122.2:n.605+4A>G | |
| NM_001353194.2:c.443+4A>G | NP_001340123.1:n.443+4A>G | |
| NM_001353195.2:c.254+4A>G | NP_001340124.1:n.254+4A>G | |
| NM_001353196.2:c.515+4A>G | NP_001340125.1:n.515+4A>G | |
| NM_001353197.2:c.443+4A>G | NP_001340126.2:n.443+4A>G | |
| NM_001353198.2:c.443+4A>G | NP_001340127.2:n.443+4A>G | |
| NM_001353199.2:c.254+4A>G | NP_001340128.2:n.254+4A>G | |
| NM_001353200.2:c.149+4A>G | NP_001340129.1:n.149+4A>G | |
| NM_001374689.1:c.443+4A>G | NP_001361618.1:n.443+4A>G | |
| NM_001374690.1:c.605+4A>G | NP_001361619.1:n.605+4A>G | |
| NM_001374691.1:c.254+4A>G | NP_001361620.1:n.254+4A>G | |
| NM_001374692.1:c.254+4A>G | NP_001361621.1:n.254+4A>G | |
| NM_001374693.1:c.443+4A>G | NP_001361622.1:n.443+4A>G | |
| NM_001374695.1:c.149+4A>G | NP_001361624.1:n.149+4A>G | |
| NM_007171.4:c.605+4A>G | NP_009102.4:n.605+4A>G | |
| NR_148391.2:n.639+4A>G | ||
| NR_148392.2:n.791+4A>G | ||
| NR_148393.2:n.639+4A>G | ||
| NR_148394.2:n.527+4A>G | ||
| NR_148395.2:n.791+4A>G | ||
| NR_148396.2:n.420+4A>G | ||
| NR_148397.2:n.684+4A>G | ||
| NR_148398.2:n.639+4A>G | ||
| NR_148399.2:n.1031+4A>G | ||
| NR_148400.2:n.625+4A>G |