Linked Data
ClinVar Variation Id:
517435
dbSNP Id:
rs760917490
ExAC:
2:39213108 T / C
gnomAD v2:
2-39213108-T-C
gnomAD v4:
2-38985967-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38985967T>C , CM000664.2:g.38985967T>C | GRCh38 |
| NC_000002.11:g.39213108T>C , CM000664.1:g.39213108T>C | GRCh37 |
| NC_000002.10:g.39066612T>C | NCBI36 |
| NG_007530.1:g.139497A>G , LRG_754:g.139497A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685279.1:c.2626A>G | ENSP00000509424.1:p.Ile876Val | |
| ENST00000686849.1:n.650A>G | ||
| ENST00000690876.1:c.*1165A>G | ENSP00000508955.1:n.*1165A>G | |
| ENST00000692089.1:c.3399+1506A>G | ENSP00000508626.1:n.3399+1506A>G | |
| ENST00000692227.1:c.1162-604A>G | ENSP00000509138.1:n.1162-604A>G | |
| ENST00000402219.8:c.3859A>G MANE Select | ENSP00000384675.2:p.Ile1287Val | |
| ENST00000395038.6:c.3814A>G | ENSP00000378479.2:p.Ile1272Val | |
| ENST00000402219.6:c.3859A>G | ENSP00000384675.2:p.Ile1287Val | |
| ENST00000426016.5:c.3859A>G | ENSP00000387784.1:p.Ile1287Val | |
| NM_005633.3:c.3859A>G , LRG_754t1:c.3859A>G | NP_005624.2:p.Ile1287Val | |
| XM_005264515.3:c.3814A>G | XP_005264572.1:p.Ile1272Val | |
| XM_011533060.1:c.3952A>G | XP_011531362.1:p.Ile1318Val | |
| XM_011533061.1:c.3907A>G | XP_011531363.1:p.Ile1303Val | |
| XM_011533062.1:c.3838A>G | XP_011531364.1:p.Ile1280Val | |
| XM_011533063.1:c.3835A>G | XP_011531365.1:p.Ile1279Val | |
| XM_011533064.1:c.3688A>G | XP_011531366.1:p.Ile1230Val | |
| XM_011533065.1:c.3604-604A>G | XP_011531367.1:n.3604-604A>G | |
| XM_011533066.1:c.2794A>G | XP_011531368.1:p.Ile932Val | |
| XM_005264515.4:c.3814A>G | XP_005264572.1:p.Ile1272Val | |
| XM_011533062.2:c.3838A>G | XP_011531364.1:p.Ile1280Val | |
| XM_011533064.2:c.3688A>G | XP_011531366.1:p.Ile1230Val | |
| NM_001382394.1:c.3838A>G | NP_001369323.1:p.Ile1280Val | |
| NM_001382395.1:c.3814A>G | NP_001369324.1:p.Ile1272Val | |
| NM_005633.4:c.3859A>G MANE Select | NP_005624.2:p.Ile1287Val |