Linked Data
ClinVar Variation Id:
570865
dbSNP Id:
rs751861630
ExAC:
5:112178357 A / G
gnomAD v2:
5-112178357-A-G
gnomAD v3:
5-112842660-A-G
gnomAD v4:
5-112842660-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112842660A>G , CM000667.2:g.112842660A>G | GRCh38 |
| NC_000005.9:g.112178357A>G , CM000667.1:g.112178357A>G | GRCh37 |
| NC_000005.8:g.112206256A>G | NCBI36 |
| NG_008481.4:g.155140A>G , LRG_130:g.155140A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.7120A>G | ENSP00000473355.2:p.Thr2374Ala | |
| ENST00000505350.2:c.*7072A>G | ENSP00000481752.1:n.*7072A>G | |
| ENST00000507379.6:c.7012A>G | ENSP00000423224.2:p.Thr2338Ala | |
| ENST00000509732.6:c.7066A>G | ENSP00000426541.2:p.Thr2356Ala | |
| ENST00000512211.7:c.7066A>G | ENSP00000423828.3:p.Thr2356Ala | |
| ENST00000257430.9:c.7066A>G MANE Select | ENSP00000257430.4:p.Thr2356Ala | |
| ENST00000257430.8:c.7066A>G | ENSP00000257430.4:p.Thr2356Ala | |
| ENST00000508376.6:c.7066A>G | ENSP00000427089.2:p.Thr2356Ala | |
| ENST00000508624.5:c.*6388A>G | ENSP00000424265.1:n.*6388A>G | |
| ENST00000520401.1:c.230+13688A>G | ||
| NM_000038.5:c.7066A>G | NP_000029.2:p.Thr2356Ala | |
| NM_001127510.2:c.7066A>G | NP_001120982.1:p.Thr2356Ala | |
| NM_001127511.2:c.7012A>G | NP_001120983.2:p.Thr2338Ala | |
| NM_001354895.1:c.7066A>G | NP_001341824.1:p.Thr2356Ala | |
| NM_001354896.1:c.7120A>G | NP_001341825.1:p.Thr2374Ala | |
| NM_001354897.1:c.7096A>G | NP_001341826.1:p.Thr2366Ala | |
| NM_001354898.1:c.6991A>G | NP_001341827.1:p.Thr2331Ala | |
| NM_001354899.1:c.6982A>G | NP_001341828.1:p.Thr2328Ala | |
| NM_001354900.1:c.6943A>G | NP_001341829.1:p.Thr2315Ala | |
| NM_001354901.1:c.6889A>G | NP_001341830.1:p.Thr2297Ala | |
| NM_001354902.1:c.6793A>G | NP_001341831.1:p.Thr2265Ala | |
| NM_001354903.1:c.6763A>G | NP_001341832.1:p.Thr2255Ala | |
| NM_001354904.1:c.6688A>G | NP_001341833.1:p.Thr2230Ala | |
| NM_001354905.1:c.6586A>G | NP_001341834.1:p.Thr2196Ala | |
| NM_001354906.1:c.6217A>G | NP_001341835.1:p.Thr2073Ala | |
| NM_000038.6:c.7066A>G MANE Select | NP_000029.2:p.Thr2356Ala | |
| NM_001127510.3:c.7066A>G | NP_001120982.1:p.Thr2356Ala | |
| NM_001127511.3:c.7012A>G | NP_001120983.2:p.Thr2338Ala | |
| NM_001354895.2:c.7066A>G | NP_001341824.1:p.Thr2356Ala | |
| NM_001354896.2:c.7120A>G | NP_001341825.1:p.Thr2374Ala | |
| NM_001354897.2:c.7096A>G | NP_001341826.1:p.Thr2366Ala | |
| NM_001354898.2:c.6991A>G | NP_001341827.1:p.Thr2331Ala | |
| NM_001354899.2:c.6982A>G | NP_001341828.1:p.Thr2328Ala | |
| NM_001354900.2:c.6943A>G | NP_001341829.1:p.Thr2315Ala | |
| NM_001354901.2:c.6889A>G | NP_001341830.1:p.Thr2297Ala | |
| NM_001354902.2:c.6793A>G | NP_001341831.1:p.Thr2265Ala | |
| NM_001354903.2:c.6763A>G | NP_001341832.1:p.Thr2255Ala | |
| NM_001354904.2:c.6688A>G | NP_001341833.1:p.Thr2230Ala | |
| NM_001354905.2:c.6586A>G | NP_001341834.1:p.Thr2196Ala | |
| NM_001354906.2:c.6217A>G | NP_001341835.1:p.Thr2073Ala |