Linked Data
ClinVar Variation Id:
41499
dbSNP Id:
rs201522866
ExAC:
5:112173729 A / G
gnomAD v2:
5-112173729-A-G
gnomAD v3:
5-112838032-A-G
gnomAD v4:
5-112838032-A-G
COSMIC:
COSM19130
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838032A>G , CM000667.2:g.112838032A>G | GRCh38 |
| NC_000005.9:g.112173729A>G , CM000667.1:g.112173729A>G | GRCh37 |
| NC_000005.8:g.112201628A>G | NCBI36 |
| NG_008481.4:g.150512A>G , LRG_130:g.150512A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.2103A>G | ENSP00000484935.2:n.2103A>G | |
| ENST00000504915.3:c.2492A>G | ENSP00000473355.2:p.Asn831Ser | |
| ENST00000505350.2:c.*2444A>G | ENSP00000481752.1:n.*2444A>G | |
| ENST00000507379.6:c.2384A>G | ENSP00000423224.2:p.Asn795Ser | |
| ENST00000509732.6:c.2438A>G | ENSP00000426541.2:p.Asn813Ser | |
| ENST00000512211.7:c.2438A>G | ENSP00000423828.3:p.Asn813Ser | |
| ENST00000257430.9:c.2438A>G MANE Select | ENSP00000257430.4:p.Asn813Ser | |
| ENST00000257430.8:c.2438A>G | ENSP00000257430.4:p.Asn813Ser | |
| ENST00000502371.2:c.791A>G | ||
| ENST00000507379.5:c.2384A>G | ENSP00000423224.1:p.Asn795Ser | |
| ENST00000508376.6:c.2438A>G | ENSP00000427089.2:p.Asn813Ser | |
| ENST00000508624.5:c.*1760A>G | ENSP00000424265.1:n.*1760A>G | |
| ENST00000512211.6:c.2438A>G | ENSP00000423828.2:p.Asn813Ser | |
| ENST00000520401.1:c.230+9060A>G | ||
| NM_000038.5:c.2438A>G | NP_000029.2:p.Asn813Ser | |
| NM_001127510.2:c.2438A>G | NP_001120982.1:p.Asn813Ser | |
| NM_001127511.2:c.2384A>G | NP_001120983.2:p.Asn795Ser | |
| NM_001354895.1:c.2438A>G | NP_001341824.1:p.Asn813Ser | |
| NM_001354896.1:c.2492A>G | NP_001341825.1:p.Asn831Ser | |
| NM_001354897.1:c.2468A>G | NP_001341826.1:p.Asn823Ser | |
| NM_001354898.1:c.2363A>G | NP_001341827.1:p.Asn788Ser | |
| NM_001354899.1:c.2354A>G | NP_001341828.1:p.Asn785Ser | |
| NM_001354900.1:c.2315A>G | NP_001341829.1:p.Asn772Ser | |
| NM_001354901.1:c.2261A>G | NP_001341830.1:p.Asn754Ser | |
| NM_001354902.1:c.2165A>G | NP_001341831.1:p.Asn722Ser | |
| NM_001354903.1:c.2135A>G | NP_001341832.1:p.Asn712Ser | |
| NM_001354904.1:c.2060A>G | NP_001341833.1:p.Asn687Ser | |
| NM_001354905.1:c.1958A>G | NP_001341834.1:p.Asn653Ser | |
| NM_001354906.1:c.1589A>G | NP_001341835.1:p.Asn530Ser | |
| NM_000038.6:c.2438A>G MANE Select | NP_000029.2:p.Asn813Ser | |
| NM_001127510.3:c.2438A>G | NP_001120982.1:p.Asn813Ser | |
| NM_001127511.3:c.2384A>G | NP_001120983.2:p.Asn795Ser | |
| NM_001354895.2:c.2438A>G | NP_001341824.1:p.Asn813Ser | |
| NM_001354896.2:c.2492A>G | NP_001341825.1:p.Asn831Ser | |
| NM_001354897.2:c.2468A>G | NP_001341826.1:p.Asn823Ser | |
| NM_001354898.2:c.2363A>G | NP_001341827.1:p.Asn788Ser | |
| NM_001354899.2:c.2354A>G | NP_001341828.1:p.Asn785Ser | |
| NM_001354900.2:c.2315A>G | NP_001341829.1:p.Asn772Ser | |
| NM_001354901.2:c.2261A>G | NP_001341830.1:p.Asn754Ser | |
| NM_001354902.2:c.2165A>G | NP_001341831.1:p.Asn722Ser | |
| NM_001354903.2:c.2135A>G | NP_001341832.1:p.Asn712Ser | |
| NM_001354904.2:c.2060A>G | NP_001341833.1:p.Asn687Ser | |
| NM_001354905.2:c.1958A>G | NP_001341834.1:p.Asn653Ser | |
| NM_001354906.2:c.1589A>G | NP_001341835.1:p.Asn530Ser |