Linked Data
ClinVar Variation Id:
538640
dbSNP Id:
rs571364996
ExAC:
2:71886119 A / G
gnomAD v2:
2-71886119-A-G
gnomAD v3:
2-71658989-A-G
gnomAD v4:
2-71658989-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71658989A>G , CM000664.2:g.71658989A>G | GRCh38 |
| NC_000002.11:g.71886119A>G , CM000664.1:g.71886119A>G | GRCh37 |
| NC_000002.10:g.71739627A>G | NCBI36 |
| NG_008694.1:g.210367A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.2281A>G | ENSP00000513536.1:p.Ile761Val | |
| ENST00000698058.1:c.1498A>G | ENSP00000513537.1:p.Ile500Val | |
| ENST00000698059.1:c.1606A>G | ENSP00000513538.1:p.Ile536Val | |
| ENST00000258104.8:c.4750A>G MANE Plus Clinical | ENSP00000258104.3:p.Ile1584Val | |
| ENST00000410020.8:c.4867A>G MANE Select | ENSP00000386881.3:p.Ile1623Val | |
| ENST00000258104.7:c.4750A>G | ENSP00000258104.3:p.Ile1584Val | |
| ENST00000394120.6:c.4753A>G | ENSP00000377678.2:p.Ile1585Val | |
| ENST00000409366.5:c.4816A>G | ENSP00000386512.1:p.Ile1606Val | |
| ENST00000409582.7:c.4864A>G | ENSP00000386547.3:p.Ile1622Val | |
| ENST00000409651.5:c.4846A>G | ENSP00000386683.1:p.Ile1616Val | |
| ENST00000409744.5:c.4774A>G | ENSP00000386285.1:p.Ile1592Val | |
| ENST00000409762.5:c.4801A>G | ENSP00000387137.1:p.Ile1601Val | |
| ENST00000410020.7:c.4867A>G | ENSP00000386881.3:p.Ile1623Val | |
| ENST00000410041.1:c.4804A>G | ENSP00000386617.1:p.Ile1602Val | |
| ENST00000413539.6:c.4843A>G | ENSP00000407046.2:p.Ile1615Val | |
| ENST00000429174.6:c.4813A>G | ENSP00000398305.2:p.Ile1605Val | |
| ENST00000479049.6:n.1635A>G | ||
| NM_001130455.1:c.4753A>G | NP_001123927.1:p.Ile1585Val | |
| NM_001130976.1:c.4708A>G | NP_001124448.1:p.Ile1570Val | |
| NM_001130977.1:c.4771A>G | NP_001124449.1:p.Ile1591Val | |
| NM_001130978.1:c.4813A>G | NP_001124450.1:p.Ile1605Val | |
| NM_001130979.1:c.4843A>G | NP_001124451.1:p.Ile1615Val | |
| NM_001130980.1:c.4801A>G | NP_001124452.1:p.Ile1601Val | |
| NM_001130981.1:c.4864A>G | NP_001124453.1:p.Ile1622Val | |
| NM_001130982.1:c.4846A>G | NP_001124454.1:p.Ile1616Val | |
| NM_001130983.1:c.4816A>G | NP_001124455.1:p.Ile1606Val | |
| NM_001130984.1:c.4774A>G | NP_001124456.1:p.Ile1592Val | |
| NM_001130985.1:c.4804A>G | NP_001124457.1:p.Ile1602Val | |
| NM_001130986.1:c.4711A>G | NP_001124458.1:p.Ile1571Val | |
| NM_001130987.1:c.4867A>G | NP_001124459.1:p.Ile1623Val | |
| NM_003494.3:c.4750A>G | NP_003485.1:p.Ile1584Val | |
| XM_005264584.3:c.4909A>G | XP_005264641.1:p.Ile1637Val | |
| XM_005264585.3:c.4906A>G | XP_005264642.1:p.Ile1636Val | |
| XM_005264584.4:c.4909A>G | XP_005264641.1:p.Ile1637Val | |
| XM_005264585.5:c.4906A>G | XP_005264642.1:p.Ile1636Val | |
| XR_001738969.1:n.5067A>G | ||
| NM_001130987.2:c.4867A>G MANE Select | NP_001124459.1:p.Ile1623Val | |
| NM_001130455.2:c.4753A>G | NP_001123927.1:p.Ile1585Val | |
| NM_001130976.2:c.4708A>G | NP_001124448.1:p.Ile1570Val | |
| NM_001130977.2:c.4771A>G | NP_001124449.1:p.Ile1591Val | |
| NM_001130978.2:c.4813A>G | NP_001124450.1:p.Ile1605Val | |
| NM_001130979.2:c.4843A>G | NP_001124451.1:p.Ile1615Val | |
| NM_001130980.2:c.4801A>G | NP_001124452.1:p.Ile1601Val | |
| NM_001130981.2:c.4864A>G | NP_001124453.1:p.Ile1622Val | |
| NM_001130982.2:c.4846A>G | NP_001124454.1:p.Ile1616Val | |
| NM_001130983.2:c.4816A>G | NP_001124455.1:p.Ile1606Val | |
| NM_001130984.2:c.4774A>G | NP_001124456.1:p.Ile1592Val | |
| NM_001130985.2:c.4804A>G | NP_001124457.1:p.Ile1602Val | |
| NM_001130986.2:c.4711A>G | NP_001124458.1:p.Ile1571Val | |
| NM_003494.4:c.4750A>G MANE Plus Clinical | NP_003485.1:p.Ile1584Val |