Linked Data
ClinVar Variation Id:
3268
dbSNP Id:
rs121434262
COSMIC:
COSM26056
PubMed:
PMID:12434154
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193122225C>T , CM000663.2:g.193122225C>T | GRCh38 |
| NC_000001.10:g.193091355C>T , CM000663.1:g.193091355C>T | GRCh37 |
| NC_000001.9:g.191357978C>T | NCBI36 |
| NG_012691.1:g.5268C>T , LRG_507:g.5268C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.25C>T MANE Select | ENSP00000356405.4:p.Arg9Ter | |
| ENST00000635846.1:c.25C>T | ENSP00000490035.1:p.Arg9Ter | |
| ENST00000643006.1:c.25C>T | ENSP00000496633.1:p.Arg9Ter | |
| ENST00000643784.1:c.25C>T | ENSP00000494944.1:p.Arg9Ter | |
| ENST00000648071.1:c.25C>T | ENSP00000497513.1:p.Arg9Ter | |
| ENST00000649606.1:n.38C>T | ||
| ENST00000649895.1:n.243C>T | ||
| ENST00000650197.1:c.25C>T | ENSP00000496929.1:p.Arg9Ter | |
| ENST00000367435.3:c.25C>T | ENSP00000356405.3:p.Arg9Ter | |
| NM_024529.4:c.25C>T , LRG_507t1:c.25C>T | NP_078805.3:p.Arg9Ter | |
| XM_006711537.2:c.25C>T | XP_006711600.1:p.Arg9Ter | |
| XM_006711537.4:c.25C>T | XP_006711600.1:p.Arg9Ter | |
| XR_001738350.1:n.1432G>A | ||
| NM_024529.5:c.25C>T MANE Select | NP_078805.3:p.Arg9Ter |