Linked Data
ClinVar Variation Id:
211316
dbSNP Id:
rs797045657
gnomAD v2:
12-49426847-T-C
gnomAD v3:
12-49033064-T-C
gnomAD v4:
12-49033064-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49033064T>C , CM000674.2:g.49033064T>C | GRCh38 |
| NC_000012.11:g.49426847T>C , CM000674.1:g.49426847T>C | GRCh37 |
| NC_000012.10:g.47713114T>C | NCBI36 |
| NG_027827.1:g.27261A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683543.2:c.11641A>G | ENSP00000506726.1:p.Met3881Val | |
| ENST00000685166.1:c.11650A>G | ENSP00000509386.1:p.Met3884Val | |
| ENST00000685554.1:c.1201A>G | ENSP00000508640.1:p.Met401Val | |
| ENST00000687201.1:c.3220A>G | ENSP00000510037.1:p.Met1074Val | |
| ENST00000692637.1:c.11638A>G | ENSP00000509666.1:p.Met3880Val | |
| ENST00000692841.1:c.3120A>G | ENSP00000508711.1:n.3120A>G | |
| ENST00000301067.12:c.11641A>G MANE Select | ENSP00000301067.7:p.Met3881Val | |
| ENST00000301067.11:c.11641A>G | ENSP00000301067.7:p.Met3881Val | |
| NM_003482.3:c.11641A>G | NP_003473.3:p.Met3881Val | |
| XM_005269162.3:c.11641A>G | XP_005269219.1:p.Met3881Val | |
| XM_006719614.2:c.11650A>G | XP_006719677.1:p.Met3884Val | |
| XM_006719616.2:c.11638A>G | XP_006719679.1:p.Met3880Val | |
| XM_011538770.1:c.11650A>G | XP_011537072.1:p.Met3884Val | |
| XM_011538771.1:c.11647A>G | XP_011537073.1:p.Met3883Val | |
| XM_011538772.1:c.11641A>G | XP_011537074.1:p.Met3881Val | |
| XM_011538773.1:c.11638A>G | XP_011537075.1:p.Met3880Val | |
| XM_011538774.1:c.11629A>G | XP_011537076.1:p.Met3877Val | |
| XM_011538775.1:c.11650A>G | XP_011537077.1:p.Met3884Val | |
| XM_011538776.1:c.11557A>G | XP_011537078.1:p.Met3853Val | |
| XR_944740.1:n.13970A>G | ||
| XM_005269162.4:c.11641A>G | XP_005269219.1:p.Met3881Val | |
| XM_006719614.4:c.11650A>G | XP_006719677.1:p.Met3884Val | |
| XM_006719616.3:c.11638A>G | XP_006719679.1:p.Met3880Val | |
| XM_011538770.2:c.11650A>G | XP_011537072.1:p.Met3884Val | |
| XM_011538771.2:c.11647A>G | XP_011537073.1:p.Met3883Val | |
| XM_011538772.2:c.11641A>G | XP_011537074.1:p.Met3881Val | |
| XM_011538773.2:c.11638A>G | XP_011537075.1:p.Met3880Val | |
| XM_011538774.2:c.11629A>G | XP_011537076.1:p.Met3877Val | |
| XM_011538776.2:c.11557A>G | XP_011537078.1:p.Met3853Val | |
| XR_001748874.1:n.12959A>G | ||
| NM_003482.4:c.11641A>G MANE Select | NP_003473.3:p.Met3881Val |