Linked Data
ClinVar Variation Id:
142939
dbSNP Id:
rs587782835
gnomAD v2:
19-1223163-C-T
gnomAD v3:
19-1223164-C-T
gnomAD v4:
19-1223164-C-T
COSMIC:
COSM21358
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1223164C>T , CM000681.2:g.1223164C>T | GRCh38 |
| NC_000019.9:g.1223163C>T , CM000681.1:g.1223163C>T | GRCh37 |
| NC_000019.8:g.1174163C>T | NCBI36 |
| NG_007460.2:g.38758C>T , LRG_319:g.38758C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.1100C>T | ENSP00000490268.2:p.Thr367Met | |
| ENST00000585748.3:c.728C>T | ENSP00000477641.2:p.Thr243Met | |
| ENST00000585851.2:c.926C>T | ENSP00000467912.2:p.Thr309Met | |
| ENST00000326873.12:c.1100C>T MANE Select | ENSP00000324856.6:p.Thr367Met | |
| ENST00000652231.1:c.1100C>T | ENSP00000498804.1:p.Thr367Met | |
| ENST00000326873.11:c.1100C>T | ENSP00000324856.6:p.Thr367Met | |
| ENST00000585465.2:n.17C>T | ||
| ENST00000586243.5:c.1100C>T | ENSP00000467240.2:p.Thr367Met | |
| ENST00000589152.5:n.1798C>T | ||
| NM_000455.4:c.1100C>T , LRG_319t1:c.1100C>T | NP_000446.1:p.Thr367Met | |
| XM_005259617.1:c.1100C>T | XP_005259674.1:p.Thr367Met | |
| XM_005259618.3:c.1100C>T | XP_005259675.1:p.Thr367Met | |
| XM_011528209.1:c.878C>T | XP_011526511.1:p.Thr293Met | |
| XR_936204.1:n.1876C>T | ||
| XM_005259617.3:c.1100C>T | XP_005259674.1:p.Thr367Met | |
| XM_011528209.2:c.878C>T | XP_011526511.1:p.Thr293Met | |
| XR_001753738.2:n.1906C>T | ||
| XR_001753739.1:n.1906C>T | ||
| XR_001753740.2:n.1876C>T | ||
| NM_000455.5:c.1100C>T MANE Select | NP_000446.1:p.Thr367Met |