Linked Data
COSMIC:
COSM1487872
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6182128A>T , CM000668.2:g.6182128A>T | GRCh38 |
| NC_000006.11:g.6182361A>T , CM000668.1:g.6182361A>T | GRCh37 |
| NC_000006.10:g.6127360A>T | NCBI36 |
| NG_008107.1:g.143564T>A , LRG_549:g.143564T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.1319T>A MANE Select | ENSP00000264870.3:p.Leu440His | |
| ENST00000264870.7:c.1319T>A | ENSP00000264870.3:p.Leu440His | |
| NM_000129.3:c.1319T>A , LRG_549t1:c.1319T>A | NP_000120.2:p.Leu440His | |
| XM_006715010.2:c.1319T>A | XP_006715073.1:p.Leu440His | |
| XM_011514342.1:c.1481T>A | XP_011512644.1:p.Leu494His | |
| NM_000129.4:c.1319T>A MANE Select | NP_000120.2:p.Leu440His |