Linked Data
ClinVar Variation Id:
166325
ClinVar RCV Id:
RCV000152511
RCV000172730
RCV000476516
RCV001133208
RCV001133210
RCV001133207
RCV001133209
RCV001133206
RCV001798487
RCV002460048
dbSNP Id:
rs150667217
ExAC:
2:179644851 A / G
gnomAD v2:
2-179644851-A-G
gnomAD v3:
2-178780124-A-G
gnomAD v4:
2-178780124-A-G
PubMed:
PMID:23861362
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178780124A>G , CM000664.2:g.178780124A>G | GRCh38 |
| NC_000002.11:g.179644851A>G , CM000664.1:g.179644851A>G | GRCh37 |
| NC_000002.10:g.179353096A>G | NCBI36 |
| NG_011618.3:g.55679T>C , LRG_391:g.55679T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.3605T>C | ENSP00000343764.6:p.Val1202Ala | |
| ENST00000342175.11:c.3467T>C | ENSP00000340554.6:p.Val1156Ala | |
| ENST00000359218.10:c.3467T>C | ENSP00000352154.5:p.Val1156Ala | |
| ENST00000360870.10:c.3605T>C MANE Plus Clinical | ENSP00000354117.4:p.Val1202Ala | |
| ENST00000342175.10:c.3467T>C | ENSP00000340554.6:p.Val1156Ala | |
| ENST00000342992.10:c.3605T>C | ENSP00000343764.6:p.Val1202Ala | |
| ENST00000359218.9:c.3467T>C | ENSP00000352154.5:p.Val1156Ala | |
| ENST00000360870.9:c.3605T>C | ENSP00000354117.4:p.Val1202Ala | |
| ENST00000460472.6:c.3467T>C | ENSP00000434586.1:p.Val1156Ala | |
| ENST00000589042.5:c.3605T>C MANE Select | ENSP00000467141.1:p.Val1202Ala | |
| ENST00000591111.5:c.3605T>C | ENSP00000465570.1:p.Val1202Ala | |
| ENST00000615779.4:c.3605T>C | ENSP00000483597.1:p.Val1202Ala | |
| NM_001256850.1:c.3605T>C | NP_001243779.1:p.Val1202Ala | |
| NM_001267550.2:c.3605T>C MANE Select | NP_001254479.2:p.Val1202Ala | |
| NM_003319.4:c.3467T>C | NP_003310.4:p.Val1156Ala | |
| NM_133378.4:c.3605T>C | NP_596869.4:p.Val1202Ala | |
| NM_133379.4:c.3605T>C , LRG_391t2:c.3605T>C | NP_596870.2:p.Val1202Ala | |
| NM_133432.3:c.3467T>C | NP_597676.3:p.Val1156Ala | |
| NM_133437.4:c.3467T>C | NP_597681.4:p.Val1156Ala | |
| XM_011511729.1:c.3653T>C | XP_011510031.1:p.Val1218Ala | |
| XM_011511730.1:c.3653T>C | XP_011510032.1:p.Val1218Ala | |
| XM_011511731.1:c.3512T>C | XP_011510033.1:p.Val1171Ala | |
| XM_011511732.1:c.3650T>C | XP_011510034.1:p.Val1217Ala | |
| XM_017004819.1:c.3608T>C | XP_016860308.1:p.Val1203Ala | |
| XM_017004820.1:c.3608T>C | XP_016860309.1:p.Val1203Ala | |
| XM_017004821.1:c.3605T>C | XP_016860310.1:p.Val1202Ala | |
| XM_017004822.1:c.3608T>C | XP_016860311.1:p.Val1203Ala | |
| XM_017004823.1:c.3608T>C | XP_016860312.1:p.Val1203Ala | |
| XM_024453094.1:c.3608T>C | XP_024308862.1:p.Val1203Ala | |
| XM_024453095.1:c.3608T>C | XP_024308863.1:p.Val1203Ala | |
| XM_024453096.1:c.3608T>C | XP_024308864.1:p.Val1203Ala | |
| XM_024453097.1:c.3608T>C | XP_024308865.1:p.Val1203Ala | |
| XM_024453098.1:c.3608T>C | XP_024308866.1:p.Val1203Ala | |
| XM_024453099.1:c.3608T>C | XP_024308867.1:p.Val1203Ala | |
| NM_133379.5:c.3605T>C MANE Plus Clinical | NP_596870.2:p.Val1202Ala |