Linked Data
ClinVar Variation Id:
5670
ClinVar RCV Id:
RCV000006024
dbSNP Id:
rs121908516
PubMed:
PMID:15248095
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.32136964A>T , CM000664.2:g.32136964A>T | GRCh38 |
| NC_000002.11:g.32362033A>T , CM000664.1:g.32362033A>T | GRCh37 |
| NC_000002.10:g.32215537A>T | NCBI36 |
| NG_008730.1:g.78354A>T , LRG_714:g.78354A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704289.1:c.*1069A>T | ENSP00000515816.1:n.*1069A>T | |
| ENST00000315285.9:c.1409A>T MANE Select | ENSP00000320885.3:p.Asp470Val | |
| ENST00000621856.2:c.1406A>T | ENSP00000482496.2:p.Asp469Val | |
| ENST00000642281.1:c.1146A>T | ||
| ENST00000642455.1:c.1310A>T | ENSP00000493827.1:p.Asp437Val | |
| ENST00000642751.1:c.1183A>T | ||
| ENST00000642999.1:c.1151A>T | ENSP00000496589.1:p.Asp384Val | |
| ENST00000643327.1:c.481-145A>T | ||
| ENST00000643334.1:c.989A>T | ||
| ENST00000644408.1:c.1285A>T | ||
| ENST00000644954.1:c.1055A>T | ENSP00000494312.1:p.Asp352Val | |
| ENST00000645159.1:n.2146A>T | ||
| ENST00000645671.1:c.859A>T | ||
| ENST00000645730.1:c.593-145A>T | ||
| ENST00000646082.1:c.1055A>T | ||
| ENST00000646571.1:c.1313A>T | ENSP00000495015.1:p.Asp438Val | |
| ENST00000647007.1:n.1101A>T | ||
| ENST00000647133.1:c.909A>T | ||
| ENST00000315285.7:c.1409A>T | ENSP00000320885.3:p.Asp470Val | |
| ENST00000345662.5:c.1313A>T | ENSP00000340817.1:p.Asp438Val | |
| ENST00000615843.4:c.1409A>T | ENSP00000480893.1:p.Asp470Val | |
| ENST00000621856.1:c.1151A>T | ENSP00000482496.1:p.Asp384Val | |
| NM_014946.3:c.1409A>T , LRG_714t1:c.1409A>T | NP_055761.2:p.Asp470Val | |
| NM_199436.1:c.1313A>T | NP_955468.1:p.Asp438Val | |
| XM_005264516.3:c.1406A>T | XP_005264573.1:p.Asp469Val | |
| XM_011533067.1:c.1409A>T | XP_011531369.1:p.Asp470Val | |
| NM_001363823.1:c.1406A>T | NP_001350752.1:p.Asp469Val | |
| NM_001363875.1:c.1310A>T | NP_001350804.1:p.Asp437Val | |
| XM_005264516.5:c.1406A>T | XP_005264573.1:p.Asp469Val | |
| XM_011533067.2:c.1409A>T | XP_011531369.1:p.Asp470Val | |
| XM_017004778.2:c.1313A>T | XP_016860267.1:p.Asp438Val | |
| NM_001363823.2:c.1406A>T | NP_001350752.1:p.Asp469Val | |
| NM_001363875.2:c.1310A>T | NP_001350804.1:p.Asp437Val | |
| NM_001377959.1:c.1313A>T | NP_001364888.1:p.Asp438Val | |
| NM_014946.4:c.1409A>T MANE Select | NP_055761.2:p.Asp470Val | |
| NM_199436.2:c.1313A>T | NP_955468.1:p.Asp438Val |