Linked Data
ClinVar Variation Id:
331407
dbSNP Id:
rs551649582
ExAC:
2:152349875 T / C
gnomAD v2:
2-152349875-T-C
gnomAD v3:
2-151493361-T-C
gnomAD v4:
2-151493361-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.151493361T>C , CM000664.2:g.151493361T>C | GRCh38 |
| NC_000002.11:g.152349875T>C , CM000664.1:g.152349875T>C | GRCh37 |
| NC_000002.10:g.152058121T>C | NCBI36 |
| NG_009382.2:g.246127A>G , LRG_202:g.246127A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000434685.6:c.3075-867A>G (NEB) | ||
| ENST00000688578.1:c.1356A>G (NEB) | ||
| ENST00000690043.1:c.6470+800A>G (NEB) | ||
| ENST00000693000.1:n.2657-867A>G (NEB) | ||
| ENST00000397345.8:c.24757A>G (NEB) MANE Select | ENSP00000380505.3:p.Ile8253Val | |
| ENST00000427231.7:c.24757A>G (NEB) MANE Plus Clinical | ENSP00000416578.2:p.Ile8253Val | |
| ENST00000172853.14:c.19189A>G (NEB) | ENSP00000172853.10:p.Ile6397Val | |
| ENST00000397337.6:c.1158A>G (NEB) | ||
| ENST00000397345.7:c.24757A>G (NEB) | ENSP00000380505.3:p.Ile8253Val | |
| ENST00000409198.5:c.19189A>G (NEB) | ENSP00000386259.1:p.Ile6397Val | |
| ENST00000413693.5:c.8211+800A>G (NEB) | ENSP00000410961.1:n.8211+800A>G | |
| ENST00000421461.6:c.1193A>G (NEB) | ||
| ENST00000427231.6:c.24757A>G (NEB) | ENSP00000416578.2:p.Ile8253Val | |
| ENST00000434685.5:c.1487+800A>G (NEB) | ||
| ENST00000454583.6:c.2656-1868T>C (RIF1) | ||
| ENST00000457745.1:n.481-1868T>C (RIF1) | ||
| ENST00000498015.2:n.226-867A>G (NEB) | ||
| ENST00000603639.5:c.24757A>G (NEB) | ENSP00000473894.1:p.Ile8253Val | |
| ENST00000604864.5:c.24757A>G (NEB) | ENSP00000474498.1:p.Ile8253Val | |
| ENST00000618972.4:c.24862A>G (NEB) | ENSP00000484342.1:p.Ile8288Val | |
| NM_001164507.1:c.24757A>G (NEB) | NP_001157979.1:p.Ile8253Val | |
| NM_001164508.1:c.24757A>G (NEB) | NP_001157980.1:p.Ile8253Val | |
| NM_001271208.1:c.24862A>G , LRG_202t1:c.24862A>G (NEB) | NP_001258137.1:p.Ile8288Val | |
| NM_004543.4:c.19189A>G (NEB) | NP_004534.2:p.Ile6397Val | |
| XM_005246590.1:c.24664A>G (NEB) | XP_005246647.1:p.Ile8222Val | |
| XM_005246591.1:c.24664A>G (NEB) | XP_005246648.1:p.Ile8222Val | |
| XM_005246592.1:c.24664A>G (NEB) | XP_005246649.1:p.Ile8222Val | |
| XM_005246593.1:c.24664A>G (NEB) | XP_005246650.1:p.Ile8222Val | |
| XM_005246594.1:c.24664A>G (NEB) | XP_005246651.1:p.Ile8222Val | |
| XM_005246595.1:c.24664A>G (NEB) | XP_005246652.1:p.Ile8222Val | |
| XM_005246596.1:c.24571A>G (NEB) | XP_005246653.1:p.Ile8191Val | |
| XM_005246597.1:c.24571A>G (NEB) | XP_005246654.1:p.Ile8191Val | |
| XM_005246598.1:c.24579+800A>G (NEB) | XP_005246655.1:n.24579+800A>G | |
| XM_005246599.1:c.24478A>G (NEB) | XP_005246656.1:p.Ile8160Val | |
| XM_005246600.1:c.24478A>G (NEB) | XP_005246657.1:p.Ile8160Val | |
| XM_005246601.1:c.24385A>G (NEB) | XP_005246658.1:p.Ile8129Val | |
| XM_005246602.1:c.24385A>G (NEB) | XP_005246659.1:p.Ile8129Val | |
| XM_005246603.1:c.24292A>G (NEB) | XP_005246660.1:p.Ile8098Val | |
| XM_005246604.1:c.24292A>G (NEB) | XP_005246661.1:p.Ile8098Val | |
| XM_005246606.1:c.24292A>G (NEB) | XP_005246663.1:p.Ile8098Val | |
| XM_005246608.1:c.24199A>G (NEB) | XP_005246665.1:p.Ile8067Val | |
| XM_005246610.1:c.24106A>G (NEB) | XP_005246667.1:p.Ile8036Val | |
| XM_005246611.1:c.24106A>G (NEB) | XP_005246668.1:p.Ile8036Val | |
| XM_005246612.1:c.24028A>G (NEB) | XP_005246669.1:p.Ile8010Val | |
| XM_005246613.1:c.24028A>G (NEB) | XP_005246670.1:p.Ile8010Val | |
| XM_005246615.1:c.24021+800A>G (NEB) | XP_005246672.1:n.24021+800A>G | |
| XM_005246617.1:c.21841A>G (NEB) | XP_005246674.1:p.Ile7281Val | |
| XM_006712541.1:c.24292A>G (NEB) | XP_006712604.1:p.Ile8098Val | |
| XM_006712542.1:c.24292A>G (NEB) | XP_006712605.1:p.Ile8098Val | |
| XM_011511224.1:c.24664A>G (NEB) | XP_011509526.1:p.Ile8222Val | |
| XM_011511225.1:c.24013A>G (NEB) | XP_011509527.1:p.Ile8005Val | |
| XM_011511226.1:c.22570A>G (NEB) | XP_011509528.1:p.Ile7524Val | |
| XM_011511227.1:c.20383A>G (NEB) | XP_011509529.1:p.Ile6795Val | |
| XR_922954.1:n.7839-1868T>C (RIF1) | ||
| XR_922955.1:n.7838+10026T>C (RIF1) | ||
| XR_922956.1:n.7839-1868T>C (RIF1) | ||
| XR_922957.1:n.7839-4425T>C (RIF1) | ||
| XM_005246590.2:c.24664A>G (NEB) | XP_005246647.1:p.Ile8222Val | |
| XM_005246591.2:c.24664A>G (NEB) | XP_005246648.1:p.Ile8222Val | |
| XM_005246592.2:c.24664A>G (NEB) | XP_005246649.1:p.Ile8222Val | |
| XM_005246593.2:c.24664A>G (NEB) | XP_005246650.1:p.Ile8222Val | |
| XM_005246594.2:c.24664A>G (NEB) | XP_005246651.1:p.Ile8222Val | |
| XM_005246596.2:c.24571A>G (NEB) | XP_005246653.1:p.Ile8191Val | |
| XM_005246597.2:c.24571A>G (NEB) | XP_005246654.1:p.Ile8191Val | |
| XM_005246598.2:c.24579+800A>G (NEB) | XP_005246655.1:n.24579+800A>G | |
| XM_005246599.2:c.24478A>G (NEB) | XP_005246656.1:p.Ile8160Val | |
| XM_005246601.2:c.24385A>G (NEB) | XP_005246658.1:p.Ile8129Val | |
| XM_005246602.2:c.24385A>G (NEB) | XP_005246659.1:p.Ile8129Val | |
| XM_005246603.2:c.24292A>G (NEB) | XP_005246660.1:p.Ile8098Val | |
| XM_005246604.2:c.24292A>G (NEB) | XP_005246661.1:p.Ile8098Val | |
| XM_005246606.2:c.24292A>G (NEB) | XP_005246663.1:p.Ile8098Val | |
| XM_005246608.2:c.24199A>G (NEB) | XP_005246665.1:p.Ile8067Val | |
| XM_005246610.2:c.24106A>G (NEB) | XP_005246667.1:p.Ile8036Val | |
| XM_005246611.2:c.24106A>G (NEB) | XP_005246668.1:p.Ile8036Val | |
| XM_005246612.2:c.24028A>G (NEB) | XP_005246669.1:p.Ile8010Val | |
| XM_005246613.2:c.24028A>G (NEB) | XP_005246670.1:p.Ile8010Val | |
| XM_005246615.2:c.24021+800A>G (NEB) | XP_005246672.1:n.24021+800A>G | |
| XM_005246617.2:c.21841A>G (NEB) | XP_005246674.1:p.Ile7281Val | |
| XM_006712541.2:c.24292A>G (NEB) | XP_006712604.1:p.Ile8098Val | |
| XM_006712542.2:c.24292A>G (NEB) | XP_006712605.1:p.Ile8098Val | |
| XM_011511225.2:c.24013A>G (NEB) | XP_011509527.1:p.Ile8005Val | |
| XM_011511226.2:c.22570A>G (NEB) | XP_011509528.1:p.Ile7524Val | |
| XM_011511227.2:c.20383A>G (NEB) | XP_011509529.1:p.Ile6795Val | |
| XM_017004177.1:c.24646A>G (NEB) | XP_016859666.1:p.Ile8216Val | |
| XM_017004178.1:c.24571A>G (NEB) | XP_016859667.1:p.Ile8191Val | |
| XM_017004179.1:c.24292A>G (NEB) | XP_016859668.1:p.Ile8098Val | |
| XM_017004180.1:c.24292A>G (NEB) | XP_016859669.1:p.Ile8098Val | |
| XM_017004181.1:c.24199A>G (NEB) | XP_016859670.1:p.Ile8067Val | |
| XM_017004182.1:c.24106A>G (NEB) | XP_016859671.1:p.Ile8036Val | |
| XM_017004183.1:c.24013A>G (NEB) | XP_016859672.1:p.Ile8005Val | |
| XM_017004184.1:c.24021+800A>G (NEB) | XP_016859673.1:n.24021+800A>G | |
| XM_017004185.1:c.23743-867A>G (NEB) | XP_016859674.1:n.23743-867A>G | |
| XR_001738811.2:n.8214-1868T>C (RIF1) | ||
| XR_001738812.2:n.8214-1868T>C (RIF1) | ||
| XR_001738813.2:n.8214-4425T>C (RIF1) | ||
| XR_001738814.2:n.8214-6044T>C (RIF1) | ||
| XR_001738815.2:n.8214-9673T>C (RIF1) | ||
| XR_001738816.2:n.8213+10026T>C (RIF1) | ||
| XR_001738817.2:n.8213+10026T>C (RIF1) | ||
| NM_001271208.2:c.24862A>G (NEB) | NP_001258137.2:p.Ile8288Val | |
| NM_004543.5:c.19189A>G (NEB) | NP_004534.3:p.Ile6397Val | |
| NM_001164507.2:c.24757A>G (NEB) MANE Plus Clinical | NP_001157979.2:p.Ile8253Val | |
| NM_001164508.2:c.24757A>G (NEB) MANE Select | NP_001157980.2:p.Ile8253Val |