Linked Data
ClinVar Variation Id:
41206
dbSNP Id:
rs267606577
gnomAD v2:
11-67258274-A-G
gnomAD v4:
11-67490803-A-G
PubMed:
PMID:22720333
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67490803A>G , CM000673.2:g.67490803A>G | GRCh38 |
| NC_000011.9:g.67258274A>G , CM000673.1:g.67258274A>G | GRCh37 |
| NC_000011.8:g.67014850A>G | NCBI36 |
| NG_008969.1:g.12770A>G , LRG_460:g.12770A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000525341.2:c.1110A>G | ||
| ENST00000528641.7:c.614A>G | ENSP00000434982.3:p.Tyr205Cys | |
| ENST00000529797.2:n.1645A>G | ||
| ENST00000682324.1:c.469-194A>G | ENSP00000508017.1:n.469-194A>G | |
| ENST00000682659.1:c.434A>G | ENSP00000507351.1:p.Tyr145Cys | |
| ENST00000682699.1:c.803A>G | ENSP00000507935.1:p.Tyr268Cys | |
| ENST00000683237.1:c.795A>G | ENSP00000507343.1:p.Leu265= | |
| ENST00000683856.1:c.626A>G | ENSP00000507979.1:p.Tyr209Cys | |
| ENST00000684006.1:c.792A>G | ENSP00000507269.1:p.Leu264= | |
| ENST00000684657.1:c.623A>G | ENSP00000507961.1:p.Tyr208Cys | |
| ENST00000279146.8:c.803A>G MANE Select | ENSP00000279146.3:p.Tyr268Cys | |
| ENST00000279146.7:c.803A>G | ENSP00000279146.3:p.Tyr268Cys | |
| ENST00000528641.6:c.614A>G | ENSP00000434982.2:p.Tyr205Cys | |
| NM_001302959.1:c.626A>G | NP_001289888.1:p.Tyr209Cys | |
| NM_001302960.1:c.795A>G | NP_001289889.1:p.Leu265= | |
| NM_003977.3:c.803A>G | NP_003968.3:p.Tyr268Cys | |
| XM_024448761.1:c.803A>G | XP_024304529.1:p.Tyr268Cys | |
| NM_003977.4:c.803A>G MANE Select | NP_003968.3:p.Tyr268Cys | |
| NM_001302960.2:c.795A>G | NP_001289889.1:p.Leu265= | |
| NM_001302959.2:c.626A>G | NP_001289888.1:p.Tyr209Cys |