Linked Data
COSMIC:
COSN17568145
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.154227274T>C , CM000667.2:g.154227274T>C | GRCh38 |
| NC_000005.9:g.153606834T>C , CM000667.1:g.153606834T>C | GRCh37 |
| NC_000005.8:g.153587027T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297107.11:c.159+36249T>C MANE Select | ENSP00000297107.6:n.159+36249T>C | |
| ENST00000297107.10:c.159+36249T>C | ENSP00000297107.6:n.159+36249T>C | |
| ENST00000377661.2:c.159+36249T>C | ENSP00000366889.2:n.159+36249T>C | |
| ENST00000425427.6:c.159+36249T>C | ENSP00000415210.2:n.159+36249T>C | |
| ENST00000520647.5:c.159+36249T>C | ENSP00000428573.1:n.159+36249T>C | |
| ENST00000521781.5:n.150+9125T>C | ||
| NM_198321.3:c.159+36249T>C | NP_938080.1:n.159+36249T>C | |
| NM_198321.4:c.159+36249T>C MANE Select | NP_938080.1:n.159+36249T>C |