Linked Data
ClinVar Variation Id:
2033921
ClinVar RCV Id:
RCV002872740
MyVariant Identifiers:
chr17:g.8140717G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8237399G>A , CM000679.2:g.8237399G>A | GRCh38 |
| NC_000017.10:g.8140717G>A , CM000679.1:g.8140717G>A | GRCh37 |
| NC_000017.9:g.8081442G>A | NCBI36 |
| NG_032148.1:g.15697C>T | |
| NG_032148.2:g.15697C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580299.2:c.768C>T | ENSP00000462607.2:p.Val256= | |
| ENST00000581729.2:c.768C>T | ENSP00000462720.2:p.Val256= | |
| ENST00000581967.2:n.790C>T | ||
| ENST00000583254.2:n.182C>T | ||
| ENST00000699849.1:c.-130C>T | ENSP00000514647.1:n.-130C>T | |
| ENST00000699850.1:n.56-1057C>T | ||
| ENST00000699851.1:n.790C>T | ||
| ENST00000699852.1:c.768C>T | ENSP00000514648.1:p.Val256= | |
| ENST00000699853.1:c.768C>T | ENSP00000514649.1:p.Val256= | |
| ENST00000699854.1:n.561C>T | ||
| ENST00000699855.1:n.790C>T | ||
| ENST00000699856.1:c.768C>T | ENSP00000514650.1:p.Val256= | |
| ENST00000699857.1:n.776C>T | ||
| ENST00000699858.1:c.768C>T | ENSP00000514651.1:p.Val256= | |
| ENST00000699859.1:c.768C>T | ENSP00000514652.1:p.Val256= | |
| ENST00000699861.1:n.790C>T | ||
| ENST00000699862.1:n.655C>T | ||
| ENST00000449476.7:c.663C>T | ENSP00000396018.2:p.Val221= | |
| ENST00000581671.2:n.609C>T | ||
| ENST00000643543.1:c.768C>T | ENSP00000494323.1:p.Val256= | |
| ENST00000651323.1:c.768C>T MANE Select | ENSP00000498499.1:p.Val256= | |
| ENST00000315684.12:c.768C>T | ENSP00000313759.8:p.Val256= | |
| ENST00000449476.6:c.663C>T | ENSP00000396018.2:p.Val221= | |
| ENST00000581671.1:n.609C>T | ||
| NM_025099.5:c.768C>T | NP_079375.3:p.Val256= | |
| NR_046431.1:n.722C>T | ||
| XM_006721577.2:c.768C>T | XP_006721640.1:p.Val256= | |
| XM_006721578.2:c.768C>T | XP_006721641.1:p.Val256= | |
| XM_006721579.2:c.768C>T | XP_006721642.1:p.Val256= | |
| XM_011524010.1:c.663C>T | XP_011522312.1:p.Val221= | |
| XM_011524011.1:c.-134C>T | XP_011522313.1:n.-134C>T | |
| XR_429823.2:n.811C>T | ||
| XR_429824.2:n.811C>T | ||
| XR_429825.1:n.811C>T | ||
| NM_025099.6:c.768C>T MANE Select | NP_079375.3:p.Val256= | |
| XM_006721577.3:c.768C>T | XP_006721640.1:p.Val256= | |
| XM_006721578.3:c.768C>T | XP_006721641.1:p.Val256= | |
| XM_011524010.2:c.663C>T | XP_011522312.1:p.Val221= | |
| XM_011524011.2:c.-134C>T | XP_011522313.1:n.-134C>T | |
| XR_001752639.1:n.811C>T | ||
| XR_001752640.1:n.811C>T | ||
| XR_001752641.1:n.811C>T | ||
| XR_001752642.1:n.811C>T | ||
| XR_001752643.1:n.811C>T | ||
| XR_001752644.1:n.811C>T | ||
| XR_002958073.1:n.811C>T | ||
| XR_429823.3:n.811C>T | ||
| XR_429824.3:n.811C>T | ||
| NR_046431.2:n.683C>T |