Linked Data
COSMIC:
COSN24349231
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4863163dup , CM000666.2:g.4863163dup | GRCh38 |
| NC_000004.11:g.4864890dup , CM000666.1:g.4864890dup | GRCh37 |
| NC_000004.10:g.4915791dup | NCBI36 |
| NG_008121.1:g.8499dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.*20dup MANE Select | ENSP00000372170.4:n.*20dup | |
| ENST00000382723.4:c.*20dup | ENSP00000372170.4:n.*20dup | |
| NM_002448.3:c.*20dup MANE Select | NP_002439.2:n.*20dup |