Linked Data
ClinVar Variation Id:
3114132
ClinVar RCV Id:
RCV004411483
dbSNP Id:
rs1434598584
gnomAD v3:
2-201724430-C-T
gnomAD v4:
2-201724430-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.201724430C>T , CM000664.2:g.201724430C>T | GRCh38 |
| NC_000002.11:g.202589153C>T , CM000664.1:g.202589153C>T | GRCh37 |
| NC_000002.10:g.202297398C>T | NCBI36 |
| NG_008775.1:g.61743G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264276.11:c.3377G>A MANE Select | ENSP00000264276.6:p.Cys1126Tyr | |
| ENST00000439495.6:c.1055G>A | ENSP00000403832.2:p.Cys352Tyr | |
| ENST00000482891.6:n.4145G>A | ||
| ENST00000494017.6:n.1109G>A | ||
| ENST00000679409.1:c.1055G>A | ENSP00000506531.1:p.Cys352Tyr | |
| ENST00000679416.1:n.4881G>A | ||
| ENST00000679435.1:c.3377G>A | ENSP00000505218.1:p.Cys1126Tyr | |
| ENST00000679516.1:c.3377G>A | ENSP00000505187.1:p.Cys1126Tyr | |
| ENST00000679618.1:c.*465G>A | ENSP00000506274.1:n.*465G>A | |
| ENST00000679630.1:n.5226G>A | ||
| ENST00000679686.1:n.3491G>A | ||
| ENST00000679701.1:n.6369G>A | ||
| ENST00000679916.1:c.3377G>A | ENSP00000506172.1:p.Cys1126Tyr | |
| ENST00000680000.1:c.3377G>A | ENSP00000506173.1:p.Cys1126Tyr | |
| ENST00000680135.1:c.*1341G>A | ENSP00000506211.1:n.*1341G>A | |
| ENST00000680149.1:c.3377G>A | ENSP00000506497.1:p.Cys1126Tyr | |
| ENST00000680163.1:c.3377G>A | ENSP00000505092.1:p.Cys1126Tyr | |
| ENST00000680174.1:n.4068G>A | ||
| ENST00000680236.1:c.*438G>A | ENSP00000506212.1:n.*438G>A | |
| ENST00000680497.1:c.3479G>A | ENSP00000505954.1:p.Cys1160Tyr | |
| ENST00000680508.1:c.3377G>A | ENSP00000505749.1:p.Cys1126Tyr | |
| ENST00000680569.1:c.*1088G>A | ENSP00000505522.1:n.*1088G>A | |
| ENST00000680630.1:n.3809G>A | ||
| ENST00000680634.1:n.21-3941G>A | ||
| ENST00000680722.1:n.1177G>A | ||
| ENST00000680723.1:n.4160G>A | ||
| ENST00000680726.1:c.3377G>A | ENSP00000505505.1:p.Cys1126Tyr | |
| ENST00000680737.1:n.3648G>A | ||
| ENST00000680759.1:c.3377G>A | ENSP00000505848.1:p.Cys1126Tyr | |
| ENST00000680814.1:c.3377G>A | ENSP00000505710.1:p.Cys1126Tyr | |
| ENST00000680828.1:c.*949G>A | ENSP00000505249.1:n.*949G>A | |
| ENST00000680861.1:c.3377G>A | ENSP00000505043.1:p.Cys1126Tyr | |
| ENST00000680927.1:c.3377G>A | ENSP00000505473.1:p.Cys1126Tyr | |
| ENST00000680939.1:n.3719G>A | ||
| ENST00000681152.1:c.3377G>A | ENSP00000505388.1:p.Cys1126Tyr | |
| ENST00000681250.1:c.*94G>A | ENSP00000505684.1:n.*94G>A | |
| ENST00000681256.1:c.*1395G>A | ENSP00000505446.1:n.*1395G>A | |
| ENST00000681279.1:n.4145G>A | ||
| ENST00000681303.1:c.3377G>A | ENSP00000505576.1:p.Cys1126Tyr | |
| ENST00000681307.1:n.4490G>A | ||
| ENST00000681461.1:n.4145G>A | ||
| ENST00000681495.1:c.917G>A | ENSP00000506085.1:p.Cys306Tyr | |
| ENST00000681558.1:c.1055G>A | ENSP00000505568.1:p.Cys352Tyr | |
| ENST00000681619.1:c.3377G>A | ENSP00000505071.1:p.Cys1126Tyr | |
| ENST00000681716.1:c.*1088G>A | ENSP00000505078.1:n.*1088G>A | |
| ENST00000681758.1:n.3719G>A | ||
| ENST00000681768.1:c.*1041G>A | ENSP00000506311.1:n.*1041G>A | |
| ENST00000681808.1:c.3377G>A | ENSP00000505219.1:p.Cys1126Tyr | |
| ENST00000264276.10:c.3377G>A | ENSP00000264276.6:p.Cys1126Tyr | |
| ENST00000439495.5:c.1338G>A | ||
| ENST00000482891.5:n.3517G>A | ||
| ENST00000489440.5:n.198G>A | ||
| NM_020919.3:c.3377G>A | NP_065970.2:p.Cys1126Tyr | |
| XM_005246709.2:c.3377G>A | XP_005246766.1:p.Cys1126Tyr | |
| XM_006712654.1:c.3377G>A | XP_006712717.1:p.Cys1126Tyr | |
| XM_006712655.2:c.1313G>A | XP_006712718.1:p.Cys438Tyr | |
| XM_011511530.1:c.3038G>A | XP_011509832.1:p.Cys1013Tyr | |
| XM_011511531.1:c.3377G>A | XP_011509833.1:p.Cys1126Tyr | |
| XR_922974.1:n.3512G>A | ||
| XM_006712654.3:c.3377G>A | XP_006712717.1:p.Cys1126Tyr | |
| XM_006712655.3:c.1313G>A | XP_006712718.1:p.Cys438Tyr | |
| XM_017004569.2:c.3377G>A | XP_016860058.1:p.Cys1126Tyr | |
| XM_017004570.2:c.3377G>A | XP_016860059.1:p.Cys1126Tyr | |
| XM_017004572.2:c.995G>A | XP_016860061.1:p.Cys332Tyr | |
| XM_024453024.1:c.3038G>A | XP_024308792.1:p.Cys1013Tyr | |
| XM_024453025.1:c.1313G>A | XP_024308793.1:p.Cys438Tyr | |
| XR_001738864.2:n.3512G>A | ||
| XR_001738865.2:n.3512G>A | ||
| XR_001738866.2:n.3512G>A | ||
| XR_001738867.2:n.3512G>A | ||
| XR_002959320.1:n.2568G>A | ||
| NM_020919.4:c.3377G>A MANE Select | NP_065970.2:p.Cys1126Tyr |