Linked Data
ClinVar Variation Id:
142466
dbSNP Id:
rs374625279
gnomAD v2:
5-112177540-A-G
gnomAD v3:
5-112841843-A-G
gnomAD v4:
5-112841843-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112841843A>G , CM000667.2:g.112841843A>G | GRCh38 |
| NC_000005.9:g.112177540A>G , CM000667.1:g.112177540A>G | GRCh37 |
| NC_000005.8:g.112205439A>G | NCBI36 |
| NG_008481.4:g.154323A>G , LRG_130:g.154323A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.6303A>G | ENSP00000473355.2:p.Ile2101Met | |
| ENST00000505350.2:c.*6255A>G | ENSP00000481752.1:n.*6255A>G | |
| ENST00000507379.6:c.6195A>G | ENSP00000423224.2:p.Ile2065Met | |
| ENST00000509732.6:c.6249A>G | ENSP00000426541.2:p.Ile2083Met | |
| ENST00000512211.7:c.6249A>G | ENSP00000423828.3:p.Ile2083Met | |
| ENST00000257430.9:c.6249A>G MANE Select | ENSP00000257430.4:p.Ile2083Met | |
| ENST00000257430.8:c.6249A>G | ENSP00000257430.4:p.Ile2083Met | |
| ENST00000508376.6:c.6249A>G | ENSP00000427089.2:p.Ile2083Met | |
| ENST00000508624.5:c.*5571A>G | ENSP00000424265.1:n.*5571A>G | |
| ENST00000520401.1:c.230+12871A>G | ||
| NM_000038.5:c.6249A>G | NP_000029.2:p.Ile2083Met | |
| NM_001127510.2:c.6249A>G | NP_001120982.1:p.Ile2083Met | |
| NM_001127511.2:c.6195A>G | NP_001120983.2:p.Ile2065Met | |
| NM_001354895.1:c.6249A>G | NP_001341824.1:p.Ile2083Met | |
| NM_001354896.1:c.6303A>G | NP_001341825.1:p.Ile2101Met | |
| NM_001354897.1:c.6279A>G | NP_001341826.1:p.Ile2093Met | |
| NM_001354898.1:c.6174A>G | NP_001341827.1:p.Ile2058Met | |
| NM_001354899.1:c.6165A>G | NP_001341828.1:p.Ile2055Met | |
| NM_001354900.1:c.6126A>G | NP_001341829.1:p.Ile2042Met | |
| NM_001354901.1:c.6072A>G | NP_001341830.1:p.Ile2024Met | |
| NM_001354902.1:c.5976A>G | NP_001341831.1:p.Ile1992Met | |
| NM_001354903.1:c.5946A>G | NP_001341832.1:p.Ile1982Met | |
| NM_001354904.1:c.5871A>G | NP_001341833.1:p.Ile1957Met | |
| NM_001354905.1:c.5769A>G | NP_001341834.1:p.Ile1923Met | |
| NM_001354906.1:c.5400A>G | NP_001341835.1:p.Ile1800Met | |
| NM_000038.6:c.6249A>G MANE Select | NP_000029.2:p.Ile2083Met | |
| NM_001127510.3:c.6249A>G | NP_001120982.1:p.Ile2083Met | |
| NM_001127511.3:c.6195A>G | NP_001120983.2:p.Ile2065Met | |
| NM_001354895.2:c.6249A>G | NP_001341824.1:p.Ile2083Met | |
| NM_001354896.2:c.6303A>G | NP_001341825.1:p.Ile2101Met | |
| NM_001354897.2:c.6279A>G | NP_001341826.1:p.Ile2093Met | |
| NM_001354898.2:c.6174A>G | NP_001341827.1:p.Ile2058Met | |
| NM_001354899.2:c.6165A>G | NP_001341828.1:p.Ile2055Met | |
| NM_001354900.2:c.6126A>G | NP_001341829.1:p.Ile2042Met | |
| NM_001354901.2:c.6072A>G | NP_001341830.1:p.Ile2024Met | |
| NM_001354902.2:c.5976A>G | NP_001341831.1:p.Ile1992Met | |
| NM_001354903.2:c.5946A>G | NP_001341832.1:p.Ile1982Met | |
| NM_001354904.2:c.5871A>G | NP_001341833.1:p.Ile1957Met | |
| NM_001354905.2:c.5769A>G | NP_001341834.1:p.Ile1923Met | |
| NM_001354906.2:c.5400A>G | NP_001341835.1:p.Ile1800Met |