Linked Data
ClinVar Variation Id:
296136
dbSNP Id:
rs142487190
ExAC:
1:231411199 C / T
gnomAD v2:
1-231411199-C-T
gnomAD v3:
1-231275453-C-T
gnomAD v4:
1-231275453-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.231275453C>T , CM000663.2:g.231275453C>T | GRCh38 |
| NC_000001.10:g.231411199C>T , CM000663.1:g.231411199C>T | GRCh37 |
| NC_000001.9:g.229477822C>T | NCBI36 |
| NG_008240.1:g.39281C>T | |
| NG_008240.2:g.39281C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366647.9:c.1892C>T MANE Select | ENSP00000355607.4:p.Ala631Val | |
| ENST00000644483.1:c.*1578C>T | ENSP00000496537.1:n.*1578C>T | |
| ENST00000366647.8:c.1892C>T | ENSP00000355607.4:p.Ala631Val | |
| ENST00000469332.1:n.474C>T | ||
| NM_001316350.1:c.1709C>T | NP_001303279.1:p.Ala570Val | |
| NM_014236.3:c.1892C>T | NP_055051.1:p.Ala631Val | |
| XM_005273313.3:c.1889C>T | XP_005273370.1:p.Ala630Val | |
| XM_011544303.1:c.1565C>T | XP_011542605.1:p.Ala522Val | |
| XM_011544304.1:c.1565C>T | XP_011542606.1:p.Ala522Val | |
| XM_005273313.4:c.1889C>T | XP_005273370.1:p.Ala630Val | |
| XM_011544303.3:c.1565C>T | XP_011542605.1:p.Ala522Val | |
| XM_011544304.2:c.1565C>T | XP_011542606.1:p.Ala522Val | |
| NM_014236.4:c.1892C>T MANE Select | NP_055051.1:p.Ala631Val | |
| NM_001316350.2:c.1709C>T | NP_001303279.1:p.Ala570Val |