Linked Data
ClinVar Variation Id:
183370
ClinVar RCV Id:
RCV000172947
dbSNP Id:
rs793888511
PubMed:
PMID:25972376
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49032017G>A , CM000674.2:g.49032017G>A | GRCh38 |
| NC_000012.11:g.49425800G>A , CM000674.1:g.49425800G>A | GRCh37 |
| NC_000012.10:g.47712067G>A | NCBI36 |
| NG_027827.1:g.28308C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683543.2:c.12688C>T | ENSP00000506726.1:p.Gln4230Ter | |
| ENST00000685166.1:c.12697C>T | ENSP00000509386.1:p.Gln4233Ter | |
| ENST00000685554.1:c.1752+496C>T | ENSP00000508640.1:n.1752+496C>T | |
| ENST00000692637.1:c.12685C>T | ENSP00000509666.1:p.Gln4229Ter | |
| ENST00000692841.1:c.4167C>T | ENSP00000508711.1:n.4167C>T | |
| ENST00000301067.12:c.12688C>T MANE Select | ENSP00000301067.7:p.Gln4230Ter | |
| ENST00000301067.11:c.12688C>T | ENSP00000301067.7:p.Gln4230Ter | |
| NM_003482.3:c.12688C>T | NP_003473.3:p.Gln4230Ter | |
| XM_005269162.3:c.12688C>T | XP_005269219.1:p.Gln4230Ter | |
| XM_006719614.2:c.12697C>T | XP_006719677.1:p.Gln4233Ter | |
| XM_006719616.2:c.12685C>T | XP_006719679.1:p.Gln4229Ter | |
| XM_011538770.1:c.12697C>T | XP_011537072.1:p.Gln4233Ter | |
| XM_011538771.1:c.12694C>T | XP_011537073.1:p.Gln4232Ter | |
| XM_011538772.1:c.12688C>T | XP_011537074.1:p.Gln4230Ter | |
| XM_011538773.1:c.12685C>T | XP_011537075.1:p.Gln4229Ter | |
| XM_011538774.1:c.12676C>T | XP_011537076.1:p.Gln4226Ter | |
| XM_011538775.1:c.12697C>T | XP_011537077.1:p.Gln4233Ter | |
| XM_011538776.1:c.12604C>T | XP_011537078.1:p.Gln4202Ter | |
| XR_944740.1:n.15017C>T | ||
| XM_005269162.4:c.12688C>T | XP_005269219.1:p.Gln4230Ter | |
| XM_006719614.4:c.12697C>T | XP_006719677.1:p.Gln4233Ter | |
| XM_006719616.3:c.12685C>T | XP_006719679.1:p.Gln4229Ter | |
| XM_011538770.2:c.12697C>T | XP_011537072.1:p.Gln4233Ter | |
| XM_011538771.2:c.12694C>T | XP_011537073.1:p.Gln4232Ter | |
| XM_011538772.2:c.12688C>T | XP_011537074.1:p.Gln4230Ter | |
| XM_011538773.2:c.12685C>T | XP_011537075.1:p.Gln4229Ter | |
| XM_011538774.2:c.12676C>T | XP_011537076.1:p.Gln4226Ter | |
| XM_011538776.2:c.12604C>T | XP_011537078.1:p.Gln4202Ter | |
| XR_001748874.1:n.14006C>T | ||
| NM_003482.4:c.12688C>T MANE Select | NP_003473.3:p.Gln4230Ter |