Linked Data
ClinVar Variation Id:
190976
dbSNP Id:
rs373369949
ExAC:
1:5934602 G / A
gnomAD v2:
1-5934602-G-A
gnomAD v3:
1-5874542-G-A
gnomAD v4:
1-5874542-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.5874542G>A , CM000663.2:g.5874542G>A | GRCh38 |
| NC_000001.10:g.5934602G>A , CM000663.1:g.5934602G>A | GRCh37 |
| NC_000001.9:g.5857189G>A | NCBI36 |
| NG_011724.2:g.122930C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378156.9:c.3160C>T MANE Select | ENSP00000367398.4:p.Arg1054Cys | |
| ENST00000378156.8:c.3160C>T | ENSP00000367398.4:p.Arg1054Cys | |
| ENST00000378169.7:c.*2061C>T | ENSP00000367411.3:n.*2061C>T | |
| ENST00000478423.6:n.2892C>T | ||
| ENST00000489180.6:c.*971C>T | ENSP00000423747.1:n.*971C>T | |
| NM_001291593.1:c.1621C>T | NP_001278522.1:p.Arg541Cys | |
| NM_001291594.1:c.1624C>T | NP_001278523.1:p.Arg542Cys | |
| NM_015102.4:c.3160C>T | NP_055917.1:p.Arg1054Cys | |
| NR_111987.1:n.3975C>T | ||
| XM_006710563.2:c.3160C>T | XP_006710626.1:p.Arg1054Cys | |
| XM_006710565.2:c.3160C>T | XP_006710628.1:p.Arg1054Cys | |
| XM_011541213.1:c.3157C>T | XP_011539515.1:p.Arg1053Cys | |
| XM_011541214.1:c.3118C>T | XP_011539516.1:p.Arg1040Cys | |
| XM_011541215.1:c.3049C>T | XP_011539517.1:p.Arg1017Cys | |
| XM_011541216.1:c.3160C>T | XP_011539518.1:p.Arg1054Cys | |
| XM_011541217.1:c.3160C>T | XP_011539519.1:p.Arg1054Cys | |
| XM_011541218.1:c.3160C>T | XP_011539520.1:p.Arg1054Cys | |
| XM_011541219.1:c.3106C>T | XP_011539521.1:p.Arg1036Cys | |
| XM_011541220.1:c.3160C>T | XP_011539522.1:p.Arg1054Cys | |
| XR_946604.1:n.3082+332C>T | ||
| XM_006710563.3:c.3160C>T | XP_006710626.1:p.Arg1054Cys | |
| XM_011541216.2:c.3160C>T | XP_011539518.1:p.Arg1054Cys | |
| XM_011541217.2:c.3160C>T | XP_011539519.1:p.Arg1054Cys | |
| XM_011541218.2:c.3160C>T | XP_011539520.1:p.Arg1054Cys | |
| XM_017000996.1:c.3115C>T | XP_016856485.1:p.Arg1039Cys | |
| XM_017000997.1:c.3160C>T | XP_016856486.1:p.Arg1054Cys | |
| XM_017000998.1:c.3160C>T | XP_016856487.1:p.Arg1054Cys | |
| XM_017000999.1:c.2632C>T | XP_016856488.1:p.Arg878Cys | |
| XM_017001000.2:c.2632C>T | XP_016856489.1:p.Arg878Cys | |
| XM_017001001.1:c.2362C>T | XP_016856490.1:p.Arg788Cys | |
| XM_017001003.1:c.1621C>T | XP_016856492.1:p.Arg541Cys | |
| XR_001737114.1:n.3198C>T | ||
| XR_001737115.1:n.3082+332C>T | ||
| NM_015102.5:c.3160C>T MANE Select | NP_055917.1:p.Arg1054Cys | |
| NM_001291593.2:c.1621C>T | NP_001278522.1:p.Arg541Cys | |
| NM_001291594.2:c.1624C>T | NP_001278523.1:p.Arg542Cys | |
| NR_111987.2:n.3927C>T |