Linked Data
ClinVar Variation Id:
413214
dbSNP Id:
rs878915517
gnomAD v2:
2-179545033-G-A
gnomAD v3:
2-178680306-G-A
gnomAD v4:
2-178680306-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178680306G>A , CM000664.2:g.178680306G>A | GRCh38 |
| NC_000002.11:g.179545033G>A , CM000664.1:g.179545033G>A | GRCh37 |
| NC_000002.10:g.179253278G>A | NCBI36 |
| NG_011618.3:g.155497C>T , LRG_391:g.155497C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.29634C>T | ENSP00000343764.6:p.Val9878= | |
| ENST00000342175.11:c.13859-37989C>T | ENSP00000340554.6:n.13859-37989C>T | |
| ENST00000359218.10:c.13658-37989C>T | ENSP00000352154.5:n.13658-37989C>T | |
| ENST00000342175.10:c.13859-37989C>T | ENSP00000340554.6:n.13859-37989C>T | |
| ENST00000342992.10:c.29634C>T | ENSP00000343764.6:p.Val9878= | |
| ENST00000359218.9:c.13658-37989C>T | ENSP00000352154.5:n.13658-37989C>T | |
| ENST00000414766.5:c.2014+1355C>T | ENSP00000401501.1:n.2014+1355C>T | |
| ENST00000460472.6:c.13283-37989C>T | ENSP00000434586.1:n.13283-37989C>T | |
| ENST00000589042.5:c.33366C>T MANE Select | ENSP00000467141.1:p.Val11122= | |
| ENST00000591111.5:c.32415C>T | ENSP00000465570.1:p.Val10805= | |
| ENST00000615779.4:c.32415C>T | ENSP00000483597.1:p.Val10805= | |
| NM_001256850.1:c.32415C>T | NP_001243779.1:p.Val10805= | |
| NM_001267550.2:c.33366C>T MANE Select | NP_001254479.2:p.Val11122= | |
| NM_003319.4:c.13283-37989C>T | NP_003310.4:n.13283-37989C>T | |
| NM_133378.4:c.29634C>T | NP_596869.4:p.Val9878= | |
| NM_133432.3:c.13658-37989C>T | NP_597676.3:n.13658-37989C>T | |
| NM_133437.4:c.13859-37989C>T | NP_597681.4:n.13859-37989C>T | |
| XM_011511729.1:c.32463C>T | XP_011510031.1:p.Val10821= | |
| XM_011511730.1:c.13469-37989C>T | XP_011510032.1:n.13469-37989C>T | |
| XM_011511731.1:c.13328-37989C>T | XP_011510033.1:n.13328-37989C>T | |
| XM_017004819.1:c.32418C>T | XP_016860308.1:p.Val10806= | |
| XM_017004820.1:c.29637C>T | XP_016860309.1:p.Val9879= | |
| XM_017004821.1:c.29634C>T | XP_016860310.1:p.Val9878= | |
| XM_017004822.1:c.31432+1355C>T | XP_016860311.1:n.31432+1355C>T | |
| XM_017004823.1:c.13424-37989C>T | XP_016860312.1:n.13424-37989C>T | |
| XM_024453094.1:c.32418C>T | XP_024308862.1:p.Val10806= | |
| XM_024453095.1:c.32418C>T | XP_024308863.1:p.Val10806= | |
| XM_024453096.1:c.32224+1355C>T | XP_024308864.1:n.32224+1355C>T | |
| XM_024453097.1:c.31264+1355C>T | XP_024308865.1:n.31264+1355C>T | |
| XM_024453098.1:c.31183+1355C>T | XP_024308866.1:n.31183+1355C>T | |
| XM_024453099.1:c.13424-37989C>T | XP_024308867.1:n.13424-37989C>T |