Linked Data
ClinVar Variation Id:
1163872
ClinVar RCV Id:
RCV002439208
dbSNP Id:
rs1423162478
gnomAD v4:
7-117603647-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117603647A>G , CM000669.2:g.117603647A>G | GRCh38 |
| NC_000007.13:g.117243701A>G , CM000669.1:g.117243701A>G | GRCh37 |
| NC_000007.12:g.117030937A>G | NCBI36 |
| NG_016465.4:g.142864A>G , LRG_663:g.142864A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647720.2:c.2773A>G | ENSP00000497673.2:p.Thr925Ala | |
| ENST00000647978.2:c.*2487A>G | ENSP00000497658.1:n.*2487A>G | |
| ENST00000649781.2:c.2590A>G | ENSP00000497203.1:p.Thr864Ala | |
| ENST00000685018.2:c.2773A>G | ENSP00000510194.2:p.Thr925Ala | |
| ENST00000687278.2:c.2773A>G | ENSP00000509593.2:p.Thr925Ala | |
| ENST00000699585.1:c.2773A>G | ENSP00000514456.1:p.Thr925Ala | |
| ENST00000699598.1:c.2773A>G | ENSP00000514467.1:p.Thr925Ala | |
| ENST00000699599.1:c.2773A>G | ENSP00000514468.1:p.Thr925Ala | |
| ENST00000699600.1:c.2773A>G | ENSP00000514469.1:p.Thr925Ala | |
| ENST00000699601.1:c.*1073A>G | ENSP00000514470.1:n.*1073A>G | |
| ENST00000699602.1:c.2773A>G | ENSP00000514471.1:p.Thr925Ala | |
| ENST00000699604.1:c.*2597A>G | ENSP00000514472.1:n.*2597A>G | |
| ENST00000699605.1:c.2347A>G | ENSP00000514473.1:p.Thr783Ala | |
| ENST00000687278.1:c.364A>G | ENSP00000509593.1:p.Thr122Ala | |
| ENST00000003084.11:c.2773A>G MANE Select | ENSP00000003084.6:p.Thr925Ala | |
| ENST00000647720.1:c.423A>G | ||
| ENST00000648260.1:c.1555A>G | ENSP00000497957.1:p.Thr519Ala | |
| ENST00000649406.1:c.2590A>G | ENSP00000497965.1:p.Thr864Ala | |
| ENST00000649781.1:c.2590A>G | ENSP00000497203.1:p.Thr864Ala | |
| ENST00000003084.10:c.2773A>G | ENSP00000003084.6:p.Thr925Ala | |
| ENST00000426809.5:c.2683A>G | ENSP00000389119.1:p.Thr895Ala | |
| NM_000492.3:c.2773A>G , LRG_663t1:c.2773A>G | NP_000483.3:p.Thr925Ala | |
| XM_011515751.1:c.2863A>G | XP_011514053.1:p.Thr955Ala | |
| XM_011515752.1:c.2863A>G | XP_011514054.1:p.Thr955Ala | |
| XM_011515753.1:c.2530A>G | XP_011514055.1:p.Thr844Ala | |
| XM_011515754.1:c.2530A>G | XP_011514056.1:p.Thr844Ala | |
| NM_000492.4:c.2773A>G MANE Select | NP_000483.3:p.Thr925Ala |