Linked Data
ClinVar Variation Id:
856798
ClinVar RCV Id:
RCV001062338
dbSNP Id:
rs2057998063
COSMIC:
COSM5945653
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34886875G>T , CM000683.2:g.34886875G>T | GRCh38 |
| NC_000021.8:g.36259172G>T , CM000683.1:g.36259172G>T | GRCh37 |
| NC_000021.7:g.35181042G>T | NCBI36 |
| NG_011402.2:g.1102837C>A , LRG_482:g.1102837C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000675419.1:c.319C>A MANE Select | ENSP00000501943.1:p.Arg107Ser | |
| ENST00000300305.7:c.319C>A | ENSP00000300305.3:p.Arg107Ser | |
| ENST00000344691.8:c.238C>A | ENSP00000340690.4:p.Arg80Ser | |
| ENST00000358356.9:c.238C>A | ENSP00000351123.5:p.Arg80Ser | |
| ENST00000399237.6:c.283C>A | ENSP00000382182.2:p.Arg95Ser | |
| ENST00000399240.5:c.238C>A | ENSP00000382184.1:p.Arg80Ser | |
| ENST00000437180.5:c.319C>A | ENSP00000409227.1:p.Arg107Ser | |
| ENST00000455571.5:c.280C>A | ENSP00000388189.1:p.Arg94Ser | |
| ENST00000482318.5:c.59-6162C>A | ENSP00000477067.1:n.59-6162C>A | |
| NM_001001890.2:c.238C>A | NP_001001890.1:p.Arg80Ser | |
| NM_001122607.1:c.238C>A | NP_001116079.1:p.Arg80Ser | |
| NM_001754.4:c.319C>A , LRG_482t1:c.319C>A | NP_001745.2:p.Arg107Ser | |
| XM_005261068.3:c.283C>A | XP_005261125.1:p.Arg95Ser | |
| XM_005261069.3:c.319C>A | XP_005261126.1:p.Arg107Ser | |
| XM_011529766.1:c.319C>A | XP_011528068.1:p.Arg107Ser | |
| XM_011529767.1:c.280C>A | XP_011528069.1:p.Arg94Ser | |
| XM_011529768.1:c.280C>A | XP_011528070.1:p.Arg94Ser | |
| XM_011529770.1:c.319C>A | XP_011528072.1:p.Arg107Ser | |
| XR_937576.1:n.498C>A | ||
| XM_005261069.4:c.319C>A | XP_005261126.1:p.Arg107Ser | |
| XM_011529766.2:c.319C>A | XP_011528068.1:p.Arg107Ser | |
| XM_011529767.2:c.280C>A | XP_011528069.1:p.Arg94Ser | |
| XM_011529768.2:c.280C>A | XP_011528070.1:p.Arg94Ser | |
| XM_011529770.2:c.319C>A | XP_011528072.1:p.Arg107Ser | |
| XM_017028487.1:c.166C>A | XP_016883976.1:p.Arg56Ser | |
| XR_937576.2:n.545C>A | ||
| NM_001001890.3:c.238C>A | NP_001001890.1:p.Arg80Ser | |
| NM_001122607.2:c.238C>A | NP_001116079.1:p.Arg80Ser | |
| NM_001754.5:c.319C>A MANE Select | NP_001745.2:p.Arg107Ser |