Linked Data
ClinVar Variation Id:
404922
dbSNP Id:
rs577363824
ExAC:
2:179539765 C / T
gnomAD v2:
2-179539765-C-T
gnomAD v3:
2-178675038-C-T
gnomAD v4:
2-178675038-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178675038C>T , CM000664.2:g.178675038C>T | GRCh38 |
| NC_000002.11:g.179539765C>T , CM000664.1:g.179539765C>T | GRCh37 |
| NC_000002.10:g.179248010C>T | NCBI36 |
| NG_011618.3:g.160765G>A , LRG_391:g.160765G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.30709+1G>A | ENSP00000343764.6:n.30709+1G>A | |
| ENST00000342175.11:c.13859-32721G>A | ENSP00000340554.6:n.13859-32721G>A | |
| ENST00000359218.10:c.13658-32721G>A | ENSP00000352154.5:n.13658-32721G>A | |
| ENST00000342175.10:c.13859-32721G>A | ENSP00000340554.6:n.13859-32721G>A | |
| ENST00000342992.10:c.30709+1G>A | ENSP00000343764.6:n.30709+1G>A | |
| ENST00000359218.9:c.13658-32721G>A | ENSP00000352154.5:n.13658-32721G>A | |
| ENST00000414766.5:c.2267-629G>A | ENSP00000401501.1:n.2267-629G>A | |
| ENST00000460472.6:c.13283-32721G>A | ENSP00000434586.1:n.13283-32721G>A | |
| ENST00000589042.5:c.34612+1G>A MANE Select | ENSP00000467141.1:n.34612+1G>A | |
| ENST00000591111.5:c.33490+1G>A | ENSP00000465570.1:n.33490+1G>A | |
| ENST00000615779.4:c.33490+1G>A | ENSP00000483597.1:n.33490+1G>A | |
| NM_001256850.1:c.33490+1G>A | NP_001243779.1:n.33490+1G>A | |
| NM_001267550.2:c.34612+1G>A MANE Select | NP_001254479.2:n.34612+1G>A | |
| NM_003319.4:c.13283-32721G>A | NP_003310.4:n.13283-32721G>A | |
| NM_133378.4:c.30709+1G>A | NP_596869.4:n.30709+1G>A | |
| NM_133432.3:c.13658-32721G>A | NP_597676.3:n.13658-32721G>A | |
| NM_133437.4:c.13859-32721G>A | NP_597681.4:n.13859-32721G>A | |
| XM_011511729.1:c.33709+1G>A | XP_011510031.1:n.33709+1G>A | |
| XM_011511730.1:c.13469-32721G>A | XP_011510032.1:n.13469-32721G>A | |
| XM_011511731.1:c.13328-32721G>A | XP_011510033.1:n.13328-32721G>A | |
| XM_017004819.1:c.33664+1G>A | XP_016860308.1:n.33664+1G>A | |
| XM_017004820.1:c.30712+1G>A | XP_016860309.1:n.30712+1G>A | |
| XM_017004821.1:c.30709+1G>A | XP_016860310.1:n.30709+1G>A | |
| XM_017004822.1:c.31685-629G>A | XP_016860311.1:n.31685-629G>A | |
| XM_017004823.1:c.13424-32721G>A | XP_016860312.1:n.13424-32721G>A | |
| XM_024453094.1:c.33047-629G>A | XP_024308862.1:n.33047-629G>A | |
| XM_024453095.1:c.33121+1G>A | XP_024308863.1:n.33121+1G>A | |
| XM_024453096.1:c.32477-629G>A | XP_024308864.1:n.32477-629G>A | |
| XM_024453097.1:c.31517-629G>A | XP_024308865.1:n.31517-629G>A | |
| XM_024453098.1:c.31436-629G>A | XP_024308866.1:n.31436-629G>A | |
| XM_024453099.1:c.13424-32721G>A | XP_024308867.1:n.13424-32721G>A |