Linked Data
COSMIC:
COSM4103846
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36564802T>C , CM000684.2:g.36564802T>C | GRCh38 |
| NC_000022.10:g.36960849T>C , CM000684.1:g.36960849T>C | GRCh37 |
| NC_000022.9:g.35290795T>C | NCBI36 |
| NG_031861.1:g.142842A>G | |
| NG_031861.2:g.143057A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.521A>G MANE Select | ENSP00000300105.6:p.Tyr174Cys | |
| ENST00000300105.6:c.521A>G | ENSP00000300105.6:p.Tyr174Cys | |
| NM_006078.3:c.521A>G | NP_006069.1:p.Tyr174Cys | |
| NM_006078.4:c.521A>G | NP_006069.1:p.Tyr174Cys | |
| XM_017028531.2:c.263A>G | XP_016884020.1:p.Tyr88Cys | |
| NM_001379051.1:c.452A>G | NP_001365980.1:p.Tyr151Cys | |
| NM_006078.5:c.521A>G MANE Select | NP_006069.1:p.Tyr174Cys | |
| NR_166440.1:n.1887A>G |