Linked Data
ClinVar Variation Id:
195614
dbSNP Id:
rs762709199
ExAC:
1:5935086 G / A
gnomAD v2:
1-5935086-G-A
gnomAD v3:
1-5875026-G-A
gnomAD v4:
1-5875026-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.5875026G>A , CM000663.2:g.5875026G>A | GRCh38 |
| NC_000001.10:g.5935086G>A , CM000663.1:g.5935086G>A | GRCh37 |
| NC_000001.9:g.5857673G>A | NCBI36 |
| NG_011724.2:g.122446C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378156.9:c.2892C>T MANE Select | ENSP00000367398.4:p.Ala964= | |
| ENST00000378156.8:c.2892C>T | ENSP00000367398.4:p.Ala964= | |
| ENST00000378169.7:c.*1793C>T | ENSP00000367411.3:n.*1793C>T | |
| ENST00000478423.6:n.2624C>T | ||
| ENST00000489180.6:c.*703C>T | ENSP00000423747.1:n.*703C>T | |
| ENST00000506941.1:n.449C>T | ||
| NM_001291593.1:c.1353C>T | NP_001278522.1:p.Ala451= | |
| NM_001291594.1:c.1356C>T | NP_001278523.1:p.Ala452= | |
| NM_015102.4:c.2892C>T | NP_055917.1:p.Ala964= | |
| NR_111987.1:n.3707C>T | ||
| XM_006710563.2:c.2892C>T | XP_006710626.1:p.Ala964= | |
| XM_006710565.2:c.2892C>T | XP_006710628.1:p.Ala964= | |
| XM_011541213.1:c.2889C>T | XP_011539515.1:p.Ala963= | |
| XM_011541214.1:c.2850C>T | XP_011539516.1:p.Ala950= | |
| XM_011541215.1:c.2781C>T | XP_011539517.1:p.Ala927= | |
| XM_011541216.1:c.2892C>T | XP_011539518.1:p.Ala964= | |
| XM_011541217.1:c.2892C>T | XP_011539519.1:p.Ala964= | |
| XM_011541218.1:c.2892C>T | XP_011539520.1:p.Ala964= | |
| XM_011541219.1:c.2838C>T | XP_011539521.1:p.Ala946= | |
| XM_011541220.1:c.2892C>T | XP_011539522.1:p.Ala964= | |
| XR_946604.1:n.2930C>T | ||
| XM_006710563.3:c.2892C>T | XP_006710626.1:p.Ala964= | |
| XM_011541216.2:c.2892C>T | XP_011539518.1:p.Ala964= | |
| XM_011541217.2:c.2892C>T | XP_011539519.1:p.Ala964= | |
| XM_011541218.2:c.2892C>T | XP_011539520.1:p.Ala964= | |
| XM_017000996.1:c.2847C>T | XP_016856485.1:p.Ala949= | |
| XM_017000997.1:c.2892C>T | XP_016856486.1:p.Ala964= | |
| XM_017000998.1:c.2892C>T | XP_016856487.1:p.Ala964= | |
| XM_017000999.1:c.2364C>T | XP_016856488.1:p.Ala788= | |
| XM_017001000.2:c.2364C>T | XP_016856489.1:p.Ala788= | |
| XM_017001001.1:c.2094C>T | XP_016856490.1:p.Ala698= | |
| XM_017001003.1:c.1353C>T | XP_016856492.1:p.Ala451= | |
| XR_001737114.1:n.2930C>T | ||
| XR_001737115.1:n.2930C>T | ||
| NM_015102.5:c.2892C>T MANE Select | NP_055917.1:p.Ala964= | |
| NM_001291593.2:c.1353C>T | NP_001278522.1:p.Ala451= | |
| NM_001291594.2:c.1356C>T | NP_001278523.1:p.Ala452= | |
| NR_111987.2:n.3659C>T |