Linked Data
ClinVar Variation Id:
501537
dbSNP Id:
rs201527181
ExAC:
1:5947504 G / C
gnomAD v2:
1-5947504-G-C
gnomAD v3:
1-5887444-G-C
gnomAD v4:
1-5887444-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.5887444G>C , CM000663.2:g.5887444G>C | GRCh38 |
| NC_000001.10:g.5947504G>C , CM000663.1:g.5947504G>C | GRCh37 |
| NC_000001.9:g.5870091G>C | NCBI36 |
| NG_011724.2:g.110028C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378156.9:c.2327C>G MANE Select | ENSP00000367398.4:p.Pro776Arg | |
| ENST00000378156.8:c.2327C>G | ENSP00000367398.4:p.Pro776Arg | |
| ENST00000378169.7:c.*1228C>G | ENSP00000367411.3:n.*1228C>G | |
| ENST00000466897.1:c.556C>G | ||
| ENST00000478423.6:n.2059C>G | ||
| ENST00000489180.6:c.2324C>G | ENSP00000423747.1:p.Pro775Arg | |
| ENST00000622020.4:c.2324C>G | ENSP00000481831.2:p.Pro775Arg | |
| NM_001291593.1:c.788C>G | NP_001278522.1:p.Pro263Arg | |
| NM_001291594.1:c.791C>G | NP_001278523.1:p.Pro264Arg | |
| NM_015102.4:c.2327C>G | NP_055917.1:p.Pro776Arg | |
| NR_111987.1:n.2592C>G | ||
| XM_006710563.2:c.2327C>G | XP_006710626.1:p.Pro776Arg | |
| XM_006710565.2:c.2327C>G | XP_006710628.1:p.Pro776Arg | |
| XM_011541213.1:c.2324C>G | XP_011539515.1:p.Pro775Arg | |
| XM_011541214.1:c.2327C>G | XP_011539516.1:p.Pro776Arg | |
| XM_011541215.1:c.2216C>G | XP_011539517.1:p.Pro739Arg | |
| XM_011541216.1:c.2327C>G | XP_011539518.1:p.Pro776Arg | |
| XM_011541217.1:c.2327C>G | XP_011539519.1:p.Pro776Arg | |
| XM_011541218.1:c.2327C>G | XP_011539520.1:p.Pro776Arg | |
| XM_011541219.1:c.2273C>G | XP_011539521.1:p.Pro758Arg | |
| XM_011541220.1:c.2327C>G | XP_011539522.1:p.Pro776Arg | |
| XR_946604.1:n.2365C>G | ||
| XR_946605.1:n.2204C>G | ||
| XM_006710563.3:c.2327C>G | XP_006710626.1:p.Pro776Arg | |
| XM_011541216.2:c.2327C>G | XP_011539518.1:p.Pro776Arg | |
| XM_011541217.2:c.2327C>G | XP_011539519.1:p.Pro776Arg | |
| XM_011541218.2:c.2327C>G | XP_011539520.1:p.Pro776Arg | |
| XM_017000996.1:c.2324C>G | XP_016856485.1:p.Pro775Arg | |
| XM_017000997.1:c.2327C>G | XP_016856486.1:p.Pro776Arg | |
| XM_017000998.1:c.2327C>G | XP_016856487.1:p.Pro776Arg | |
| XM_017000999.1:c.1799C>G | XP_016856488.1:p.Pro600Arg | |
| XM_017001000.2:c.1799C>G | XP_016856489.1:p.Pro600Arg | |
| XM_017001001.1:c.1529C>G | XP_016856490.1:p.Pro510Arg | |
| XM_017001002.1:c.2327C>G | XP_016856491.1:p.Pro776Arg | |
| XM_017001003.1:c.788C>G | XP_016856492.1:p.Pro263Arg | |
| XR_001737114.1:n.2365C>G | ||
| XR_001737115.1:n.2365C>G | ||
| NM_015102.5:c.2327C>G MANE Select | NP_055917.1:p.Pro776Arg | |
| NM_001291593.2:c.788C>G | NP_001278522.1:p.Pro263Arg | |
| NM_001291594.2:c.791C>G | NP_001278523.1:p.Pro264Arg | |
| NR_111987.2:n.2544C>G |