Linked Data
COSMIC:
COSN7301275
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.22877764G>C , CM000678.2:g.22877764G>C | GRCh38 |
| NC_000016.9:g.22889085G>C , CM000678.1:g.22889085G>C | GRCh37 |
| NC_000016.8:g.22796586G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261374.4:c.486-37180G>C MANE Select | ENSP00000261374.3:n.486-37180G>C | |
| ENST00000261374.3:c.486-37180G>C | ENSP00000261374.3:n.486-37180G>C | |
| ENST00000473392.1:c.*287+22983G>C | ENSP00000454505.1:n.*287+22983G>C | |
| NM_006043.1:c.486-37180G>C | NP_006034.1:n.486-37180G>C | |
| NM_006043.2:c.486-37180G>C MANE Select | NP_006034.1:n.486-37180G>C |