Linked Data
ClinVar Variation Id:
2951431
ClinVar RCV Id:
RCV003805133
COSMIC:
COSM4507706
MyVariant Identifiers:
chr11:g.36614966G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.36593416G>A , CM000673.2:g.36593416G>A | GRCh38 |
| NC_000011.9:g.36614966G>A , CM000673.1:g.36614966G>A | GRCh37 |
| NC_000011.8:g.36571542G>A | NCBI36 |
| NG_007573.1:g.9821C>T , LRG_99:g.9821C>T | |
| NG_033154.1:g.3924G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000527033.6:c.753C>T | ENSP00000436895.2:p.Val251= | |
| ENST00000529083.2:c.753C>T | ENSP00000436327.2:p.Val251= | |
| ENST00000532616.2:c.753C>T | ENSP00000432174.2:p.Val251= | |
| ENST00000311485.8:c.753C>T MANE Select | ENSP00000308620.4:p.Val251= | |
| ENST00000311485.7:c.753C>T | ENSP00000308620.3:p.Val251= | |
| ENST00000524423.1:n.131+4686C>T | ||
| ENST00000618712.4:c.753C>T | ENSP00000478672.1:p.Val251= | |
| NM_000536.3:c.753C>T | NP_000527.2:p.Val251= | |
| NM_001243785.1:c.753C>T | NP_001230714.1:p.Val251= | |
| NM_001243786.1:c.753C>T | NP_001230715.1:p.Val251= | |
| NM_000536.4:c.753C>T MANE Select | NP_000527.2:p.Val251= | |
| NM_001243785.2:c.753C>T | NP_001230714.1:p.Val251= | |
| NM_001243786.2:c.753C>T | NP_001230715.1:p.Val251= |