Linked Data
COSMIC:
COSN22629460
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454197A>T , CM000679.2:g.7454197A>T | GRCh38 |
| NC_000017.10:g.7357516A>T , CM000679.1:g.7357516A>T | GRCh37 |
| NC_000017.9:g.7298240A>T | NCBI36 |
| NG_008026.1:g.14111A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.821-100A>T MANE Select | ENSP00000304290.2:n.821-100A>T | |
| ENST00000306071.6:c.821-100A>T | ENSP00000304290.2:n.821-100A>T | |
| ENST00000536404.6:c.605-100A>T | ENSP00000439209.2:n.605-100A>T | |
| ENST00000570557.5:c.484-100A>T | ||
| ENST00000573209.1:n.1765-100A>T | ||
| ENST00000576360.1:c.605-247A>T | ENSP00000459092.1:n.605-247A>T | |
| NM_000747.2:c.821-100A>T | NP_000738.2:n.821-100A>T | |
| NM_000747.3:c.821-100A>T MANE Select | NP_000738.2:n.821-100A>T |