Linked Data
ClinVar Variation Id:
751096
ClinVar RCV Id:
RCV000928122
dbSNP Id:
rs951655012
gnomAD v2:
19-33954923-G-A
gnomAD v3:
19-33464017-G-A
gnomAD v4:
19-33464017-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33464017G>A , CM000681.2:g.33464017G>A | GRCh38 |
| NC_000019.9:g.33954923G>A , CM000681.1:g.33954923G>A | GRCh37 |
| NC_000019.8:g.38646763G>A | NCBI36 |
| NG_013358.1:g.62877C>T | |
| NG_013358.2:g.62877C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000588328.7:c.594C>T | ENSP00000468516.4:p.Thr198= | |
| ENST00000651646.2:c.594C>T | ENSP00000498950.2:p.Thr198= | |
| ENST00000651901.2:c.594C>T | ENSP00000498922.2:p.Thr198= | |
| ENST00000698359.1:c.549C>T | ENSP00000513682.1:p.Thr183= | |
| ENST00000698360.1:c.594C>T | ENSP00000513683.1:p.Thr198= | |
| ENST00000698361.1:c.594C>T | ENSP00000513684.1:p.Thr198= | |
| ENST00000698362.1:c.594C>T | ENSP00000513685.1:p.Thr198= | |
| ENST00000698363.1:n.657C>T | ||
| ENST00000698364.1:n.657C>T | ||
| ENST00000698365.1:n.657C>T | ||
| ENST00000698426.1:c.273C>T | ENSP00000513713.1:p.Thr91= | |
| ENST00000698427.1:c.636C>T | ENSP00000513714.1:p.Thr212= | |
| ENST00000698428.1:c.273C>T | ENSP00000513715.1:p.Thr91= | |
| ENST00000698430.1:c.844C>T | ||
| ENST00000698431.1:c.331C>T | ENSP00000513717.1:n.331C>T | |
| ENST00000698432.1:c.403C>T | ||
| ENST00000698435.1:c.282C>T | ENSP00000513719.1:p.Thr94= | |
| ENST00000698436.1:c.*206C>T | ENSP00000513720.1:n.*206C>T | |
| ENST00000698437.1:n.577C>T | ||
| ENST00000698438.1:n.576C>T | ||
| ENST00000698439.1:c.451C>T | ENSP00000513721.1:n.451C>T | |
| ENST00000244137.12:c.594C>T MANE Select | ENSP00000244137.5:p.Thr198= | |
| ENST00000588328.6:c.583C>T | ||
| ENST00000590731.6:n.269C>T | ||
| ENST00000651646.1:c.592C>T | ||
| ENST00000651901.1:c.590C>T | ||
| ENST00000244137.11:c.594C>T | ENSP00000244137.5:p.Thr198= | |
| ENST00000397032.8:c.548+14029C>T | ENSP00000380226.3:n.548+14029C>T | |
| ENST00000436370.7:c.402C>T | ENSP00000391890.2:p.Thr134= | |
| ENST00000588328.5:c.85C>T | ||
| ENST00000588719.5:n.229C>T | ||
| ENST00000590408.1:c.312C>T | ||
| ENST00000590731.5:n.269C>T | ||
| ENST00000590755.6:c.421C>T | ENSP00000476667.1:n.421C>T | |
| ENST00000593163.5:n.759C>T | ||
| ENST00000609145.5:c.27C>T | ENSP00000476514.1:p.Thr9= | |
| NM_000285.3:c.594C>T | NP_000276.2:p.Thr198= | |
| NM_001166056.1:c.548+14029C>T | NP_001159528.1:n.548+14029C>T | |
| NM_001166057.1:c.402C>T | NP_001159529.1:p.Thr134= | |
| NM_000285.4:c.594C>T MANE Select | NP_000276.2:p.Thr198= | |
| NM_001166056.2:c.548+14029C>T | NP_001159528.1:n.548+14029C>T | |
| NM_001166057.2:c.402C>T | NP_001159529.1:p.Thr134= |