Linked Data
ClinVar Variation Id:
1377020
ClinVar RCV Id:
RCV001889806
dbSNP Id:
rs1565470546
gnomAD v3:
12-21906252-T-C
gnomAD v4:
12-21906252-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21906252T>C , CM000674.2:g.21906252T>C | GRCh38 |
| NC_000012.11:g.22059186T>C , CM000674.1:g.22059186T>C | GRCh37 |
| NC_000012.10:g.21950453T>C | NCBI36 |
| NG_012819.1:g.35443A>G , LRG_377:g.35443A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261201.10:c.1492A>G | ENSP00000261201.4:p.Ile498Val | |
| ENST00000682068.1:c.1492A>G | ENSP00000507226.1:p.Ile498Val | |
| ENST00000682789.1:n.1743A>G | ||
| ENST00000682879.1:c.*593A>G | ENSP00000508210.1:n.*593A>G | |
| ENST00000683105.1:c.1492A>G | ENSP00000506801.1:p.Ile498Val | |
| ENST00000683676.1:c.1492A>G | ENSP00000508167.1:p.Ile498Val | |
| ENST00000684084.1:c.1492A>G | ENSP00000507859.1:p.Ile498Val | |
| ENST00000684543.1:n.1837A>G | ||
| ENST00000261200.9:c.1492A>G MANE Select | ENSP00000261200.4:p.Ile498Val | |
| ENST00000261201.9:c.1492A>G | ENSP00000261201.4:p.Ile498Val | |
| ENST00000261200.8:c.1492A>G | ENSP00000261200.4:p.Ile498Val | |
| ENST00000261201.8:c.1492A>G | ENSP00000261201.4:p.Ile498Val | |
| ENST00000544039.5:c.481A>G | ENSP00000440521.1:p.Ile161Val | |
| NM_005691.3:c.1492A>G | NP_005682.2:p.Ile498Val | |
| NM_020297.3:c.1492A>G | NP_064693.2:p.Ile498Val | |
| XM_005253284.2:c.1492A>G | XP_005253341.1:p.Ile498Val | |
| XM_005253286.2:c.1492A>G | XP_005253343.1:p.Ile498Val | |
| XM_005253287.3:c.1492A>G | XP_005253344.1:p.Ile498Val | |
| XM_005253288.2:c.1492A>G | XP_005253345.1:p.Ile498Val | |
| XM_005253289.2:c.1492A>G | XP_005253346.1:p.Ile498Val | |
| XM_005253290.2:c.1492A>G | XP_005253347.1:p.Ile498Val | |
| XM_006719025.2:c.1492A>G | XP_006719088.1:p.Ile498Val | |
| XM_011520545.1:c.1492A>G | XP_011518847.1:p.Ile498Val | |
| XM_005253284.4:c.1492A>G | XP_005253341.1:p.Ile498Val | |
| XM_005253286.4:c.1492A>G | XP_005253343.1:p.Ile498Val | |
| XM_005253287.5:c.1492A>G | XP_005253344.1:p.Ile498Val | |
| XM_005253288.4:c.1492A>G | XP_005253345.1:p.Ile498Val | |
| XM_005253289.4:c.1492A>G | XP_005253346.1:p.Ile498Val | |
| XM_005253290.4:c.1492A>G | XP_005253347.1:p.Ile498Val | |
| XM_006719025.4:c.1492A>G | XP_006719088.1:p.Ile498Val | |
| XM_011520545.3:c.1492A>G | XP_011518847.1:p.Ile498Val | |
| NM_001377273.1:c.1492A>G | NP_001364202.1:p.Ile498Val | |
| NM_001377274.1:c.628A>G | NP_001364203.1:p.Ile210Val | |
| NM_005691.4:c.1492A>G | NP_005682.2:p.Ile498Val | |
| NM_020297.4:c.1492A>G MANE Select | NP_064693.2:p.Ile498Val |