Linked Data
ClinVar Variation Id:
291052
dbSNP Id:
rs375090704
ExAC:
1:5935076 C / T
gnomAD v2:
1-5935076-C-T
gnomAD v3:
1-5875016-C-T
gnomAD v4:
1-5875016-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.5875016C>T , CM000663.2:g.5875016C>T | GRCh38 |
| NC_000001.10:g.5935076C>T , CM000663.1:g.5935076C>T | GRCh37 |
| NC_000001.9:g.5857663C>T | NCBI36 |
| NG_011724.2:g.122456G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378156.9:c.2902G>A MANE Select | ENSP00000367398.4:p.Ala968Thr | |
| ENST00000378156.8:c.2902G>A | ENSP00000367398.4:p.Ala968Thr | |
| ENST00000378169.7:c.*1803G>A | ENSP00000367411.3:n.*1803G>A | |
| ENST00000478423.6:n.2634G>A | ||
| ENST00000489180.6:c.*713G>A | ENSP00000423747.1:n.*713G>A | |
| ENST00000506941.1:n.459G>A | ||
| NM_001291593.1:c.1363G>A | NP_001278522.1:p.Ala455Thr | |
| NM_001291594.1:c.1366G>A | NP_001278523.1:p.Ala456Thr | |
| NM_015102.4:c.2902G>A | NP_055917.1:p.Ala968Thr | |
| NR_111987.1:n.3717G>A | ||
| XM_006710563.2:c.2902G>A | XP_006710626.1:p.Ala968Thr | |
| XM_006710565.2:c.2902G>A | XP_006710628.1:p.Ala968Thr | |
| XM_011541213.1:c.2899G>A | XP_011539515.1:p.Ala967Thr | |
| XM_011541214.1:c.2860G>A | XP_011539516.1:p.Ala954Thr | |
| XM_011541215.1:c.2791G>A | XP_011539517.1:p.Ala931Thr | |
| XM_011541216.1:c.2902G>A | XP_011539518.1:p.Ala968Thr | |
| XM_011541217.1:c.2902G>A | XP_011539519.1:p.Ala968Thr | |
| XM_011541218.1:c.2902G>A | XP_011539520.1:p.Ala968Thr | |
| XM_011541219.1:c.2848G>A | XP_011539521.1:p.Ala950Thr | |
| XM_011541220.1:c.2902G>A | XP_011539522.1:p.Ala968Thr | |
| XR_946604.1:n.2940G>A | ||
| XM_006710563.3:c.2902G>A | XP_006710626.1:p.Ala968Thr | |
| XM_011541216.2:c.2902G>A | XP_011539518.1:p.Ala968Thr | |
| XM_011541217.2:c.2902G>A | XP_011539519.1:p.Ala968Thr | |
| XM_011541218.2:c.2902G>A | XP_011539520.1:p.Ala968Thr | |
| XM_017000996.1:c.2857G>A | XP_016856485.1:p.Ala953Thr | |
| XM_017000997.1:c.2902G>A | XP_016856486.1:p.Ala968Thr | |
| XM_017000998.1:c.2902G>A | XP_016856487.1:p.Ala968Thr | |
| XM_017000999.1:c.2374G>A | XP_016856488.1:p.Ala792Thr | |
| XM_017001000.2:c.2374G>A | XP_016856489.1:p.Ala792Thr | |
| XM_017001001.1:c.2104G>A | XP_016856490.1:p.Ala702Thr | |
| XM_017001003.1:c.1363G>A | XP_016856492.1:p.Ala455Thr | |
| XR_001737114.1:n.2940G>A | ||
| XR_001737115.1:n.2940G>A | ||
| NM_015102.5:c.2902G>A MANE Select | NP_055917.1:p.Ala968Thr | |
| NM_001291593.2:c.1363G>A | NP_001278522.1:p.Ala455Thr | |
| NM_001291594.2:c.1366G>A | NP_001278523.1:p.Ala456Thr | |
| NR_111987.2:n.3669G>A |