Linked Data
ClinVar Variation Id:
219535
dbSNP Id:
rs202199891
ExAC:
5:112163666 T / C
gnomAD v2:
5-112163666-T-C
gnomAD v3:
5-112827969-T-C
gnomAD v4:
5-112827969-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112827969T>C , CM000667.2:g.112827969T>C | GRCh38 |
| NC_000005.9:g.112163666T>C , CM000667.1:g.112163666T>C | GRCh37 |
| NC_000005.8:g.112191565T>C | NCBI36 |
| NG_008481.4:g.140449T>C , LRG_130:g.140449T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.1408+5978T>C | ENSP00000484935.2:n.1408+5978T>C | |
| ENST00000504915.3:c.1643T>C | ENSP00000473355.2:p.Val548Ala | |
| ENST00000505084.2:n.1645T>C | ||
| ENST00000505350.2:c.*1595T>C | ENSP00000481752.1:n.*1595T>C | |
| ENST00000507379.6:c.1535T>C | ENSP00000423224.2:p.Val512Ala | |
| ENST00000509732.6:c.1589T>C | ENSP00000426541.2:p.Val530Ala | |
| ENST00000512211.7:c.1589T>C | ENSP00000423828.3:p.Val530Ala | |
| ENST00000257430.9:c.1589T>C MANE Select | ENSP00000257430.4:p.Val530Ala | |
| ENST00000257430.8:c.1589T>C | ENSP00000257430.4:p.Val530Ala | |
| ENST00000502371.2:c.96+5978T>C | ||
| ENST00000504915.2:c.278T>C | ENSP00000473355.1:p.Val93Ala | |
| ENST00000505084.1:n.76T>C | ||
| ENST00000507379.5:c.1535T>C | ENSP00000423224.1:p.Val512Ala | |
| ENST00000508376.6:c.1589T>C | ENSP00000427089.2:p.Val530Ala | |
| ENST00000508624.5:c.*911T>C | ENSP00000424265.1:n.*911T>C | |
| ENST00000512211.6:c.1589T>C | ENSP00000423828.2:p.Val530Ala | |
| ENST00000520401.1:c.76T>C | ||
| NM_000038.5:c.1589T>C | NP_000029.2:p.Val530Ala | |
| NM_001127510.2:c.1589T>C | NP_001120982.1:p.Val530Ala | |
| NM_001127511.2:c.1535T>C | NP_001120983.2:p.Val512Ala | |
| NM_001354895.1:c.1589T>C | NP_001341824.1:p.Val530Ala | |
| NM_001354896.1:c.1643T>C | NP_001341825.1:p.Val548Ala | |
| NM_001354897.1:c.1619T>C | NP_001341826.1:p.Val540Ala | |
| NM_001354898.1:c.1514T>C | NP_001341827.1:p.Val505Ala | |
| NM_001354899.1:c.1505T>C | NP_001341828.1:p.Val502Ala | |
| NM_001354900.1:c.1466T>C | NP_001341829.1:p.Val489Ala | |
| NM_001354901.1:c.1412T>C | NP_001341830.1:p.Val471Ala | |
| NM_001354902.1:c.1316T>C | NP_001341831.1:p.Val439Ala | |
| NM_001354903.1:c.1286T>C | NP_001341832.1:p.Val429Ala | |
| NM_001354904.1:c.1211T>C | NP_001341833.1:p.Val404Ala | |
| NM_001354905.1:c.1109T>C | NP_001341834.1:p.Val370Ala | |
| NM_001354906.1:c.740T>C | NP_001341835.1:p.Val247Ala | |
| NM_000038.6:c.1589T>C MANE Select | NP_000029.2:p.Val530Ala | |
| NM_001127510.3:c.1589T>C | NP_001120982.1:p.Val530Ala | |
| NM_001127511.3:c.1535T>C | NP_001120983.2:p.Val512Ala | |
| NM_001354895.2:c.1589T>C | NP_001341824.1:p.Val530Ala | |
| NM_001354896.2:c.1643T>C | NP_001341825.1:p.Val548Ala | |
| NM_001354897.2:c.1619T>C | NP_001341826.1:p.Val540Ala | |
| NM_001354898.2:c.1514T>C | NP_001341827.1:p.Val505Ala | |
| NM_001354899.2:c.1505T>C | NP_001341828.1:p.Val502Ala | |
| NM_001354900.2:c.1466T>C | NP_001341829.1:p.Val489Ala | |
| NM_001354901.2:c.1412T>C | NP_001341830.1:p.Val471Ala | |
| NM_001354902.2:c.1316T>C | NP_001341831.1:p.Val439Ala | |
| NM_001354903.2:c.1286T>C | NP_001341832.1:p.Val429Ala | |
| NM_001354904.2:c.1211T>C | NP_001341833.1:p.Val404Ala | |
| NM_001354905.2:c.1109T>C | NP_001341834.1:p.Val370Ala | |
| NM_001354906.2:c.740T>C | NP_001341835.1:p.Val247Ala |