Linked Data
ClinVar Variation Id:
161378
dbSNP Id:
rs148540135
ExAC:
19:39070725 C / T
gnomAD v2:
19-39070725-C-T
gnomAD v3:
19-38580085-C-T
gnomAD v4:
19-38580085-C-T
COSMIC:
COSM1564444
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38580085C>T , CM000681.2:g.38580085C>T | GRCh38 |
| NC_000019.9:g.39070725C>T , CM000681.1:g.39070725C>T | GRCh37 |
| NC_000019.8:g.43762565C>T | NCBI36 |
| NG_008866.1:g.151386C>T , LRG_766:g.151386C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.1404C>T | ||
| ENST00000688602.1:c.2801C>T | ||
| ENST00000689936.1:c.2773C>T | ||
| ENST00000359596.8:c.14468C>T MANE Select | ENSP00000352608.2:p.Thr4823Met | |
| ENST00000355481.8:c.14453C>T | ENSP00000347667.3:p.Thr4818Met | |
| ENST00000359596.7:c.14468C>T | ENSP00000352608.2:p.Thr4823Met | |
| ENST00000360985.7:c.14450C>T | ENSP00000354254.4:p.Thr4817Met | |
| NM_000540.2:c.14468C>T , LRG_766t1:c.14468C>T | NP_000531.2:p.Thr4823Met | |
| NM_001042723.1:c.14453C>T | NP_001036188.1:p.Thr4818Met | |
| XM_006723317.1:c.14450C>T | XP_006723380.1:p.Thr4817Met | |
| XM_006723319.1:c.14435C>T | XP_006723382.1:p.Thr4812Met | |
| XM_011527204.1:c.14465C>T | XP_011525506.1:p.Thr4822Met | |
| XM_011527205.1:c.14381C>T | XP_011525507.1:p.Thr4794Met | |
| XM_006723317.2:c.14450C>T | XP_006723380.1:p.Thr4817Met | |
| XM_006723319.2:c.14435C>T | XP_006723382.1:p.Thr4812Met | |
| XM_011527205.2:c.14381C>T | XP_011525507.1:p.Thr4794Met | |
| NM_000540.3:c.14468C>T MANE Select | NP_000531.2:p.Thr4823Met | |
| NM_001042723.2:c.14453C>T | NP_001036188.1:p.Thr4818Met |