Linked Data
COSMIC:
COSM4188032
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119672371T>G , CM000672.2:g.119672371T>G | GRCh38 |
| NC_000010.10:g.121431883T>G , CM000672.1:g.121431883T>G | GRCh37 |
| NC_000010.9:g.121421873T>G | NCBI36 |
| NG_016125.1:g.26002T>G , LRG_742:g.26002T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.624T>G MANE Select | ENSP00000358081.4:p.Ile208Met | |
| ENST00000369085.7:c.624T>G | ENSP00000358081.3:p.Ile208Met | |
| ENST00000450186.1:c.450T>G | ENSP00000410036.1:p.Ile150Met | |
| NM_004281.3:c.624T>G , LRG_742t1:c.624T>G | NP_004272.2:p.Ile208Met | |
| XM_005270287.1:c.624T>G | XP_005270344.1:p.Ile208Met | |
| XM_005270287.2:c.624T>G | XP_005270344.1:p.Ile208Met | |
| NM_004281.4:c.624T>G MANE Select | NP_004272.2:p.Ile208Met |