Linked Data
ClinVar Variation Id:
93257
dbSNP Id:
rs398123471
ExAC:
19:39076801 C / T
gnomAD v2:
19-39076801-C-T
gnomAD v4:
19-38586161-C-T
COSMIC:
COSM385043
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38586161C>T , CM000681.2:g.38586161C>T | GRCh38 |
| NC_000019.9:g.39076801C>T , CM000681.1:g.39076801C>T | GRCh37 |
| NC_000019.8:g.43768641C>T | NCBI36 |
| NG_008866.1:g.157462C>T , LRG_766:g.157462C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.1875C>T | ||
| ENST00000688602.1:c.3272C>T | ||
| ENST00000689936.1:c.3244C>T | ||
| ENST00000692547.1:n.332C>T | ||
| ENST00000359596.8:c.14939C>T MANE Select | ENSP00000352608.2:p.Thr4980Met | |
| ENST00000355481.8:c.14924C>T | ENSP00000347667.3:p.Thr4975Met | |
| ENST00000359596.7:c.14939C>T | ENSP00000352608.2:p.Thr4980Met | |
| ENST00000360985.7:c.14921C>T | ENSP00000354254.4:p.Thr4974Met | |
| NM_000540.2:c.14939C>T , LRG_766t1:c.14939C>T | NP_000531.2:p.Thr4980Met | |
| NM_001042723.1:c.14924C>T | NP_001036188.1:p.Thr4975Met | |
| XM_006723317.1:c.14921C>T | XP_006723380.1:p.Thr4974Met | |
| XM_006723319.1:c.14906C>T | XP_006723382.1:p.Thr4969Met | |
| XM_011527204.1:c.14936C>T | XP_011525506.1:p.Thr4979Met | |
| XM_011527205.1:c.14852C>T | XP_011525507.1:p.Thr4951Met | |
| XM_006723317.2:c.14921C>T | XP_006723380.1:p.Thr4974Met | |
| XM_006723319.2:c.14906C>T | XP_006723382.1:p.Thr4969Met | |
| XM_011527205.2:c.14852C>T | XP_011525507.1:p.Thr4951Met | |
| NM_000540.3:c.14939C>T MANE Select | NP_000531.2:p.Thr4980Met | |
| NM_001042723.2:c.14924C>T | NP_001036188.1:p.Thr4975Met |