Linked Data
ClinVar Variation Id:
550474
dbSNP Id:
rs764196171
ExAC:
4:996113 C / G
gnomAD v2:
4-996113-C-G
gnomAD v3:
4-1002325-C-G
gnomAD v4:
4-1002325-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.1002325C>G , CM000666.2:g.1002325C>G | GRCh38 |
| NC_000004.11:g.996113C>G , CM000666.1:g.996113C>G | GRCh37 |
| NC_000004.10:g.986113C>G | NCBI36 |
| NG_008103.1:g.20329C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000247933.9:c.1029C>G | ENSP00000247933.4:p.Tyr343Ter | |
| ENST00000514224.2:c.1029C>G MANE Select | ENSP00000425081.2:p.Tyr343Ter | |
| ENST00000652070.1:n.1085C>G | ||
| ENST00000247933.8:c.1029C>G | ENSP00000247933.4:p.Tyr343Ter | |
| ENST00000514224.1:c.633C>G | ENSP00000425081.1:p.Tyr211Ter | |
| ENST00000514698.5:n.1136C>G | ||
| NM_000203.4:c.1029C>G | NP_000194.2:p.Tyr343Ter | |
| NR_110313.1:n.1117C>G | ||
| XM_006713882.2:c.633C>G | XP_006713945.1:p.Tyr211Ter | |
| XM_011513459.1:c.1095C>G | XP_011511761.1:p.Tyr365Ter | |
| XM_011513460.1:c.888C>G | XP_011511762.1:p.Tyr296Ter | |
| XM_011513461.1:c.822C>G | XP_011511763.1:p.Tyr274Ter | |
| XM_011513462.1:c.741C>G | XP_011511764.1:p.Tyr247Ter | |
| XM_011513463.1:c.741C>G | XP_011511765.1:p.Tyr247Ter | |
| XR_924947.1:n.1098C>G | ||
| NM_000203.5:c.1029C>G MANE Select | NP_000194.2:p.Tyr343Ter | |
| NM_001363576.1:c.633C>G | NP_001350505.1:p.Tyr211Ter | |
| XM_011513461.2:c.822C>G | XP_011511763.1:p.Tyr274Ter | |
| XM_017008163.1:c.69C>G | XP_016863652.1:p.Tyr23Ter |