Linked Data
ClinVar Variation Id:
500975
dbSNP Id:
rs41280798
ExAC:
1:5933335 C / T
gnomAD v2:
1-5933335-C-T
gnomAD v3:
1-5873275-C-T
gnomAD v4:
1-5873275-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.5873275C>T , CM000663.2:g.5873275C>T | GRCh38 |
| NC_000001.10:g.5933335C>T , CM000663.1:g.5933335C>T | GRCh37 |
| NC_000001.9:g.5855922C>T | NCBI36 |
| NG_011724.2:g.124197G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378156.9:c.3292G>A MANE Select | ENSP00000367398.4:p.Ala1098Thr | |
| ENST00000378156.8:c.3292G>A | ENSP00000367398.4:p.Ala1098Thr | |
| ENST00000378169.7:c.*2193G>A | ENSP00000367411.3:n.*2193G>A | |
| ENST00000468253.1:n.567G>A | ||
| ENST00000478423.6:n.3024G>A | ||
| ENST00000489180.6:c.*1103G>A | ENSP00000423747.1:n.*1103G>A | |
| NM_001291593.1:c.1753G>A | NP_001278522.1:p.Ala585Thr | |
| NM_001291594.1:c.1756G>A | NP_001278523.1:p.Ala586Thr | |
| NM_015102.4:c.3292G>A | NP_055917.1:p.Ala1098Thr | |
| NR_111987.1:n.4107G>A | ||
| XM_006710563.2:c.3292G>A | XP_006710626.1:p.Ala1098Thr | |
| XM_006710565.2:c.3292G>A | XP_006710628.1:p.Ala1098Thr | |
| XM_011541213.1:c.3289G>A | XP_011539515.1:p.Ala1097Thr | |
| XM_011541214.1:c.3250G>A | XP_011539516.1:p.Ala1084Thr | |
| XM_011541215.1:c.3181G>A | XP_011539517.1:p.Ala1061Thr | |
| XM_011541216.1:c.3292G>A | XP_011539518.1:p.Ala1098Thr | |
| XM_011541217.1:c.3292G>A | XP_011539519.1:p.Ala1098Thr | |
| XM_011541218.1:c.3292G>A | XP_011539520.1:p.Ala1098Thr | |
| XM_011541219.1:c.3238G>A | XP_011539521.1:p.Ala1080Thr | |
| XM_011541220.1:c.3292G>A | XP_011539522.1:p.Ala1098Thr | |
| XR_946604.1:n.3143G>A | ||
| XM_006710563.3:c.3292G>A | XP_006710626.1:p.Ala1098Thr | |
| XM_011541216.2:c.3292G>A | XP_011539518.1:p.Ala1098Thr | |
| XM_011541217.2:c.3292G>A | XP_011539519.1:p.Ala1098Thr | |
| XM_011541218.2:c.3292G>A | XP_011539520.1:p.Ala1098Thr | |
| XM_017000996.1:c.3247G>A | XP_016856485.1:p.Ala1083Thr | |
| XM_017000997.1:c.3292G>A | XP_016856486.1:p.Ala1098Thr | |
| XM_017000998.1:c.3292G>A | XP_016856487.1:p.Ala1098Thr | |
| XM_017000999.1:c.2764G>A | XP_016856488.1:p.Ala922Thr | |
| XM_017001000.2:c.2764G>A | XP_016856489.1:p.Ala922Thr | |
| XM_017001001.1:c.2494G>A | XP_016856490.1:p.Ala832Thr | |
| XM_017001003.1:c.1753G>A | XP_016856492.1:p.Ala585Thr | |
| XR_001737114.1:n.3330G>A | ||
| XR_001737115.1:n.3143G>A | ||
| NM_015102.5:c.3292G>A MANE Select | NP_055917.1:p.Ala1098Thr | |
| NM_001291593.2:c.1753G>A | NP_001278522.1:p.Ala585Thr | |
| NM_001291594.2:c.1756G>A | NP_001278523.1:p.Ala586Thr | |
| NR_111987.2:n.4059G>A |