Linked Data
COSMIC:
COSM5540162
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47744818C>T , CM000679.2:g.47744818C>T | GRCh38 |
| NC_000017.10:g.45822184C>T , CM000679.1:g.45822184C>T | GRCh37 |
| NC_000017.9:g.43177183C>T | NCBI36 |
| NG_012166.1:g.16575C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000177694.2:c.1060C>T MANE Select | ENSP00000177694.1:p.His354Tyr | |
| ENST00000177694.1:c.1060C>T | ENSP00000177694.1:p.His354Tyr | |
| NM_013351.1:c.1060C>T | NP_037483.1:p.His354Tyr | |
| XM_011524698.1:c.1123C>T | XP_011523000.1:p.His375Tyr | |
| XM_011524699.1:c.727C>T | XP_011523001.1:p.His243Tyr | |
| NM_013351.2:c.1060C>T MANE Select | NP_037483.1:p.His354Tyr |