Linked Data
ClinVar Variation Id:
158790
dbSNP Id:
rs587783729
gnomAD v2:
12-49432396-G-A
gnomAD v4:
12-49038613-G-A
PubMed:
PMID:25972376
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49038613G>A , CM000674.2:g.49038613G>A | GRCh38 |
| NC_000012.11:g.49432396G>A , CM000674.1:g.49432396G>A | GRCh37 |
| NC_000012.10:g.47718663G>A | NCBI36 |
| NG_027827.1:g.21712C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683043.1:n.442C>T | ||
| ENST00000683543.2:c.8743C>T | ENSP00000506726.1:p.Arg2915Ter | |
| ENST00000685166.1:c.8752C>T | ENSP00000509386.1:p.Arg2918Ter | |
| ENST00000687201.1:c.307C>T | ENSP00000510037.1:p.Arg103Ter | |
| ENST00000689143.1:c.2346C>T | ENSP00000509839.1:n.2346C>T | |
| ENST00000692637.1:c.8740C>T | ENSP00000509666.1:p.Arg2914Ter | |
| ENST00000692841.1:c.307C>T | ENSP00000508711.1:p.Arg103Ter | |
| ENST00000301067.12:c.8743C>T MANE Select | ENSP00000301067.7:p.Arg2915Ter | |
| ENST00000301067.11:c.8743C>T | ENSP00000301067.7:p.Arg2915Ter | |
| ENST00000549799.1:n.385C>T | ||
| NM_003482.3:c.8743C>T | NP_003473.3:p.Arg2915Ter | |
| XM_005269162.3:c.8743C>T | XP_005269219.1:p.Arg2915Ter | |
| XM_006719614.2:c.8752C>T | XP_006719677.1:p.Arg2918Ter | |
| XM_006719616.2:c.8740C>T | XP_006719679.1:p.Arg2914Ter | |
| XM_011538770.1:c.8752C>T | XP_011537072.1:p.Arg2918Ter | |
| XM_011538771.1:c.8749C>T | XP_011537073.1:p.Arg2917Ter | |
| XM_011538772.1:c.8743C>T | XP_011537074.1:p.Arg2915Ter | |
| XM_011538773.1:c.8740C>T | XP_011537075.1:p.Arg2914Ter | |
| XM_011538774.1:c.8731C>T | XP_011537076.1:p.Arg2911Ter | |
| XM_011538775.1:c.8752C>T | XP_011537077.1:p.Arg2918Ter | |
| XM_011538776.1:c.8659C>T | XP_011537078.1:p.Arg2887Ter | |
| XR_944740.1:n.11072C>T | ||
| XM_005269162.4:c.8743C>T | XP_005269219.1:p.Arg2915Ter | |
| XM_006719614.4:c.8752C>T | XP_006719677.1:p.Arg2918Ter | |
| XM_006719616.3:c.8740C>T | XP_006719679.1:p.Arg2914Ter | |
| XM_011538770.2:c.8752C>T | XP_011537072.1:p.Arg2918Ter | |
| XM_011538771.2:c.8749C>T | XP_011537073.1:p.Arg2917Ter | |
| XM_011538772.2:c.8743C>T | XP_011537074.1:p.Arg2915Ter | |
| XM_011538773.2:c.8740C>T | XP_011537075.1:p.Arg2914Ter | |
| XM_011538774.2:c.8731C>T | XP_011537076.1:p.Arg2911Ter | |
| XM_011538776.2:c.8659C>T | XP_011537078.1:p.Arg2887Ter | |
| XR_001748874.1:n.10061C>T | ||
| NM_003482.4:c.8743C>T MANE Select | NP_003473.3:p.Arg2915Ter |