Linked Data
COSMIC:
COSM6117340
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.119930152G>C , CM000685.2:g.119930152G>C | GRCh38 |
| NC_000023.10:g.119064115G>C , CM000685.1:g.119064115G>C | GRCh37 |
| NC_000023.9:g.118948143G>C | NCBI36 |
| NG_021260.1:g.18621C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371410.5:c.937C>G MANE Select | ENSP00000360464.3:p.Leu313Val | |
| ENST00000652253.1:c.933C>G | ||
| ENST00000371410.4:c.937C>G | ENSP00000360464.3:p.Leu313Val | |
| ENST00000477789.5:n.1865C>G | ||
| ENST00000482407.1:n.736C>G | ||
| NM_024528.3:c.937C>G | NP_078804.2:p.Leu313Val | |
| XM_017029842.1:c.640C>G | XP_016885331.1:p.Leu214Val | |
| NM_024528.4:c.937C>G MANE Select | NP_078804.2:p.Leu313Val |