Linked Data
COSMIC:
COSM5809602
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714034T>C , CM000681.2:g.6714034T>C | GRCh38 |
| NC_000019.9:g.6714045T>C , CM000681.1:g.6714045T>C | GRCh37 |
| NC_000019.8:g.6665045T>C | NCBI36 |
| NG_009557.1:g.11618A>G , LRG_27:g.11618A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.608A>G | ENSP00000512083.1:p.Tyr203Cys | |
| ENST00000245907.11:c.731A>G MANE Select | ENSP00000245907.4:p.Tyr244Cys | |
| ENST00000245907.10:c.731A>G | ENSP00000245907.4:p.Tyr244Cys | |
| ENST00000595577.1:n.235A>G | ||
| NM_000064.3:c.731A>G | NP_000055.2:p.Tyr244Cys | |
| NM_000064.4:c.731A>G MANE Select | NP_000055.2:p.Tyr244Cys |