Linked Data
ClinVar Variation Id:
2884817
ClinVar RCV Id:
RCV003750466
dbSNP Id:
rs762515688
ExAC:
13:23928991 G / C
gnomAD v2:
13-23928991-G-C
gnomAD v4:
13-23354852-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23354852G>C , CM000675.2:g.23354852G>C | GRCh38 |
| NC_000013.10:g.23928991G>C , CM000675.1:g.23928991G>C | GRCh37 |
| NC_000013.9:g.22826991G>C | NCBI36 |
| NG_012342.1:g.83851C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.1760C>G | ENSP00000508399.1:p.Thr587Arg | |
| ENST00000682944.1:c.1760C>G | ENSP00000507173.1:p.Thr587Arg | |
| ENST00000683154.1:n.1898C>G | ||
| ENST00000683210.1:c.1760C>G | ENSP00000506739.1:p.Thr587Arg | |
| ENST00000683270.1:c.1751C>G | ENSP00000507624.1:p.Thr584Arg | |
| ENST00000683367.1:c.1751C>G | ENSP00000507780.1:p.Thr584Arg | |
| ENST00000683489.1:c.1760C>G | ENSP00000508403.1:p.Thr587Arg | |
| ENST00000683680.1:c.1760C>G | ENSP00000507223.1:p.Thr587Arg | |
| ENST00000684163.1:c.1751C>G | ENSP00000508262.1:p.Thr584Arg | |
| ENST00000684196.1:n.4117C>G | ||
| ENST00000684325.1:c.1760C>G | ENSP00000508121.1:p.Thr587Arg | |
| ENST00000684385.1:c.1760C>G | ENSP00000507855.1:p.Thr587Arg | |
| ENST00000684497.1:c.1760C>G | ENSP00000507057.1:p.Thr587Arg | |
| ENST00000382292.9:c.1760C>G MANE Select | ENSP00000371729.3:p.Thr587Arg | |
| ENST00000423156.2:c.1760C>G | ENSP00000390925.2:p.Thr587Arg | |
| ENST00000455470.6:c.1760C>G | ENSP00000406565.2:p.Thr587Arg | |
| ENST00000382292.7:c.1760C>G | ENSP00000371729.3:p.Thr587Arg | |
| ENST00000382298.7:c.1760C>G | ENSP00000371735.3:p.Thr587Arg | |
| ENST00000402364.1:c.-491C>G | ENSP00000385844.1:n.-491C>G | |
| ENST00000423156.1:c.632C>G | ENSP00000390925.1:p.Thr211Arg | |
| ENST00000455470.5:c.1458C>G | ||
| ENST00000476776.1:n.39C>G | ||
| NM_001278055.1:c.1319C>G | NP_001264984.1:p.Thr440Arg | |
| NM_014363.5:c.1760C>G | NP_055178.3:p.Thr587Arg | |
| XM_005266338.1:c.1760C>G | XP_005266395.1:p.Thr587Arg | |
| XM_011535038.1:c.1784C>G | XP_011533340.1:p.Thr595Arg | |
| XM_011535039.1:c.1751C>G | XP_011533341.1:p.Thr584Arg | |
| XM_005266338.2:c.1760C>G | XP_005266395.1:p.Thr587Arg | |
| XM_011535039.2:c.1751C>G | XP_011533341.1:p.Thr584Arg | |
| XM_017020539.1:c.1751C>G | XP_016876028.1:p.Thr584Arg | |
| XM_024449337.1:c.1760C>G | XP_024305105.1:p.Thr587Arg | |
| NM_014363.6:c.1760C>G MANE Select | NP_055178.3:p.Thr587Arg | |
| NM_001278055.2:c.1319C>G | NP_001264984.1:p.Thr440Arg |