Linked Data
ClinVar Variation Id:
515957
dbSNP Id:
rs769397483
ExAC:
11:68703880 C / T
gnomAD v2:
11-68703880-C-T
gnomAD v3:
11-68936412-C-T
gnomAD v4:
11-68936412-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68936412C>T , CM000673.2:g.68936412C>T | GRCh38 |
| NC_000011.9:g.68703880C>T , CM000673.1:g.68703880C>T | GRCh37 |
| NC_000011.8:g.68460456C>T | NCBI36 |
| NG_007976.1:g.37562C>T , LRG_250:g.37562C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255078.8:c.1932C>T MANE Select | ENSP00000255078.4:p.Asp644= | |
| ENST00000674675.1:c.176C>T | ||
| ENST00000674878.1:c.176C>T | ||
| ENST00000674955.1:c.*649C>T | ENSP00000502463.1:n.*649C>T | |
| ENST00000675118.1:c.1420C>T | ||
| ENST00000675389.1:n.207C>T | ||
| ENST00000675615.1:c.1932C>T | ENSP00000502413.1:p.Asp644= | |
| ENST00000675648.1:n.1307C>T | ||
| ENST00000675916.1:c.176C>T | ||
| ENST00000676173.1:n.2677C>T | ||
| ENST00000676182.1:c.363C>T | ||
| ENST00000676228.1:c.*1255C>T | ENSP00000502375.1:n.*1255C>T | |
| ENST00000255078.7:c.1932C>T | ENSP00000255078.3:p.Asp644= | |
| ENST00000539064.5:n.1691C>T | ||
| ENST00000543739.5:n.925C>T | ||
| ENST00000545475.1:n.528C>T | ||
| NM_002180.2:c.1932C>T , LRG_250t1:c.1932C>T | NP_002171.2:p.Asp644= | |
| XM_005273974.2:c.921C>T | XP_005274031.1:p.Asp307= | |
| XM_005273975.2:c.804C>T | XP_005274032.1:p.Asp268= | |
| XM_011544994.1:c.699C>T | XP_011543296.1:p.Asp233= | |
| XR_949903.1:n.2034C>T | ||
| XM_005273975.3:c.804C>T | XP_005274032.1:p.Asp268= | |
| XM_017017669.2:c.921C>T | XP_016873158.1:p.Asp307= | |
| XM_017017670.2:c.921C>T | XP_016873159.1:p.Asp307= | |
| XR_949903.3:n.2030C>T | ||
| NM_002180.3:c.1932C>T MANE Select | NP_002171.2:p.Asp644= |