Linked Data
ClinVar Variation Id:
1185011
ClinVar RCV Id:
RCV001543644
dbSNP Id:
rs1565853526
ERepo:
CA16020794/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102866644T>C , CM000674.2:g.102866644T>C | GRCh38 |
| NC_000012.11:g.103260422T>C , CM000674.1:g.103260422T>C | GRCh37 |
| NC_000012.10:g.101784552T>C | NCBI36 |
| NG_008690.1:g.55959A>G | |
| NG_008690.2:g.96767A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.461A>G MANE Select | ENSP00000448059.1:p.Tyr154Cys | |
| ENST00000307000.7:c.446A>G | ENSP00000303500.2:p.Tyr149Cys | |
| ENST00000549111.5:n.557A>G | ||
| ENST00000551988.5:n.530+10818A>G | ||
| ENST00000553106.5:c.461A>G | ENSP00000448059.1:p.Tyr154Cys | |
| NM_000277.1:c.461A>G | NP_000268.1:p.Tyr154Cys | |
| XM_011538422.1:c.461A>G | XP_011536724.1:p.Tyr154Cys | |
| NM_000277.2:c.461A>G | NP_000268.1:p.Tyr154Cys | |
| NM_001354304.1:c.461A>G | NP_001341233.1:p.Tyr154Cys | |
| XM_017019370.2:c.461A>G | XP_016874859.1:p.Tyr154Cys | |
| NM_000277.3:c.461A>G MANE Select | NP_000268.1:p.Tyr154Cys | |
| NM_001354304.2:c.461A>G | NP_001341233.1:p.Tyr154Cys |