Linked Data
COSMIC:
COSN20551875
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21138562A>G , CM000674.2:g.21138562A>G | GRCh38 |
| NC_000012.11:g.21291496A>G , CM000674.1:g.21291496A>G | GRCh37 |
| NC_000012.10:g.21182763A>G | NCBI36 |
| NG_011745.1:g.12369A>G , LRG_1022:g.12369A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.-61-2952A>G MANE Select | ENSP00000256958.2:n.-61-2952A>G | |
| ENST00000256958.2:c.-61-2952A>G | ENSP00000256958.2:n.-61-2952A>G | |
| ENST00000543498.5:c.281-2952A>G | ||
| ENST00000585342.5:c.485-2952A>G | ENSP00000467594.1:n.485-2952A>G | |
| ENST00000590779.5:c.491-2952A>G | ||
| ENST00000592513.1:c.472-2952A>G | ||
| NM_006446.4:c.-61-2952A>G , LRG_1022t1:c.-61-2952A>G | NP_006437.3:n.-61-2952A>G | |
| NM_006446.5:c.-61-2952A>G MANE Select | NP_006437.3:n.-61-2952A>G |