Linked Data
ClinVar Variation Id:
406249
dbSNP Id:
rs201131571
ExAC:
16:53686827 A / G
gnomAD v2:
16-53686827-A-G
gnomAD v3:
16-53652915-A-G
gnomAD v4:
16-53652915-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.53652915A>G , CM000678.2:g.53652915A>G | GRCh38 |
| NC_000016.9:g.53686827A>G , CM000678.1:g.53686827A>G | GRCh37 |
| NC_000016.8:g.52244328A>G | NCBI36 |
| NG_008991.2:g.55945T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262135.9:c.1772T>C | ENSP00000262135.4:p.Val591Ala | |
| ENST00000565343.2:n.2196T>C | ||
| ENST00000621565.5:c.1772T>C | ENSP00000480698.1:p.Val591Ala | |
| ENST00000647211.2:c.1772T>C MANE Select | ENSP00000493946.1:p.Val591Ala | |
| ENST00000680193.1:c.1772T>C | ENSP00000506379.1:p.Val591Ala | |
| ENST00000262135.8:c.1772T>C | ENSP00000262135.4:p.Val591Ala | |
| ENST00000379925.7:c.1772T>C | ENSP00000369257.3:p.Val591Ala | |
| ENST00000563746.5:c.1772T>C | ENSP00000457889.1:p.Val591Ala | |
| ENST00000564374.5:c.1772T>C | ENSP00000456534.1:p.Val591Ala | |
| ENST00000621565.4:c.1772T>C | ENSP00000480698.1:p.Val591Ala | |
| NM_001127897.1:c.1772T>C | NP_001121369.1:p.Val591Ala | |
| NM_001127897.2:c.1772T>C | NP_001121369.1:p.Val591Ala | |
| NM_001308334.1:c.1772T>C | NP_001295263.1:p.Val591Ala | |
| NM_015272.2:c.1772T>C | NP_056087.2:p.Val591Ala | |
| NM_015272.3:c.1772T>C | NP_056087.2:p.Val591Ala | |
| XM_005255867.1:c.1772T>C | XP_005255924.1:p.Val591Ala | |
| XM_005255868.1:c.1784T>C | XP_005255925.1:p.Val595Ala | |
| XM_005255871.2:c.17T>C | XP_005255928.1:p.Val6Ala | |
| XM_011522968.1:c.1772T>C | XP_011521270.1:p.Val591Ala | |
| XM_011522969.1:c.1784T>C | XP_011521271.1:p.Val595Ala | |
| XM_011522970.1:c.1784T>C | XP_011521272.1:p.Val595Ala | |
| XM_011522971.1:c.1784T>C | XP_011521273.1:p.Val595Ala | |
| XM_011522972.1:c.1784T>C | XP_011521274.1:p.Val595Ala | |
| XM_011522973.1:c.1784T>C | XP_011521275.1:p.Val595Ala | |
| XM_011522974.1:c.17T>C | XP_011521276.1:p.Val6Ala | |
| XR_933260.1:n.1816T>C | ||
| NM_001127897.3:c.1772T>C | NP_001121369.1:p.Val591Ala | |
| NM_001308334.2:c.1772T>C | NP_001295263.1:p.Val591Ala | |
| NM_001330538.1:c.1772T>C | NP_001317467.1:p.Val591Ala | |
| NM_015272.4:c.1772T>C | NP_056087.2:p.Val591Ala | |
| XM_005255868.2:c.1784T>C | XP_005255925.1:p.Val595Ala | |
| XM_011522970.2:c.1784T>C | XP_011521272.1:p.Val595Ala | |
| XM_011522971.3:c.1784T>C | XP_011521273.1:p.Val595Ala | |
| XM_011522973.3:c.1784T>C | XP_011521275.1:p.Val595Ala | |
| XM_017023094.2:c.1784T>C | XP_016878583.1:p.Val595Ala | |
| XM_017023095.2:c.1784T>C | XP_016878584.1:p.Val595Ala | |
| XM_017023096.2:c.1784T>C | XP_016878585.1:p.Val595Ala | |
| XM_017023097.2:c.1784T>C | XP_016878586.1:p.Val595Ala | |
| XM_017023098.1:c.17T>C | XP_016878587.1:p.Val6Ala | |
| XM_017023099.1:c.17T>C | XP_016878588.1:p.Val6Ala | |
| XM_017023100.2:c.*119T>C | XP_016878589.1:n.*119T>C | |
| XR_933260.3:n.1827T>C | ||
| NM_015272.5:c.1772T>C MANE Select | NP_056087.2:p.Val591Ala | |
| NM_001127897.4:c.1772T>C | NP_001121369.1:p.Val591Ala | |
| NM_001330538.2:c.1772T>C | NP_001317467.1:p.Val591Ala | |
| NM_001308334.3:c.1772T>C | NP_001295263.1:p.Val591Ala |