Linked Data
dbSNP Id:
rs104895453
gnomAD v2:
16-50756589-G-T
gnomAD v4:
16-50722678-G-T
COSMIC:
COSM703526
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.50722678G>T , CM000678.2:g.50722678G>T | GRCh38 |
| NC_000016.9:g.50756589G>T , CM000678.1:g.50756589G>T | GRCh37 |
| NC_000016.8:g.49314090G>T | NCBI36 |
| NG_007508.1:g.30540G>T , LRG_177:g.30540G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641284.2:c.2382-7140G>T | ENSP00000493088.1:n.2382-7140G>T | |
| ENST00000646677.2:c.*455G>T | ENSP00000496533.1:n.*455G>T | |
| ENST00000697425.1:c.517G>T | ||
| ENST00000697426.1:c.405G>T | ||
| ENST00000697427.1:c.321G>T | ||
| ENST00000697428.1:n.2168G>T | ||
| ENST00000641284.1:c.2382-7140G>T | ENSP00000493088.1:n.2382-7140G>T | |
| ENST00000646677.1:c.*455G>T | ENSP00000496533.1:n.*455G>T | |
| ENST00000647318.2:c.2690G>T MANE Select | ENSP00000495993.1:p.Gly897Val | |
| ENST00000300589.6:c.2771G>T | ENSP00000300589.2:p.Gly924Val | |
| ENST00000524712.5:c.265G>T | ||
| ENST00000527052.5:c.237G>T | ||
| ENST00000529633.5:c.349G>T | ||
| ENST00000534057.1:c.405G>T | ||
| ENST00000534067.5:c.501G>T | ||
| NM_001293557.1:c.2690G>T | NP_001280486.1:p.Gly897Val | |
| NM_022162.2:c.2771G>T | NP_071445.1:p.Gly924Val | |
| XM_005256084.2:c.2690G>T | XP_005256141.1:p.Gly897Val | |
| XM_006721242.2:c.2606G>T | XP_006721305.1:p.Gly869Val | |
| XM_011523257.1:c.2267G>T | XP_011521559.1:p.Gly756Val | |
| XM_011523258.1:c.2267G>T | XP_011521560.1:p.Gly756Val | |
| XM_011523259.1:c.2105G>T | XP_011521561.1:p.Gly702Val | |
| XR_429725.2:n.2612G>T | ||
| XR_429726.2:n.2528G>T | ||
| XR_933387.1:n.2808G>T | ||
| XM_005256084.4:c.2690G>T | XP_005256141.1:p.Gly897Val | |
| XM_006721242.4:c.2606G>T | XP_006721305.1:p.Gly869Val | |
| XM_011523259.2:c.2105G>T | XP_011521561.1:p.Gly702Val | |
| XM_017023535.1:c.2198G>T | XP_016879024.1:p.Gly733Val | |
| XM_017023536.1:c.2105G>T | XP_016879025.1:p.Gly702Val | |
| XM_017023537.1:c.2105G>T | XP_016879026.1:p.Gly702Val | |
| XM_017023538.1:c.2105G>T | XP_016879027.1:p.Gly702Val | |
| XR_429725.3:n.2565G>T | ||
| XR_429726.3:n.2481G>T | ||
| XR_933387.2:n.2761G>T | ||
| NM_001293557.2:c.2690G>T | NP_001280486.1:p.Gly897Val | |
| NM_001370466.1:c.2690G>T MANE Select | NP_001357395.1:p.Gly897Val | |
| NM_022162.3:c.2771G>T | NP_071445.1:p.Gly924Val | |
| NR_163434.1:n.2902G>T |