Linked Data
ClinVar Variation Id:
12983
dbSNP Id:
rs118192164
gnomAD v4:
19-38525455-C-T
COSMIC:
COSM5056609
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38525455C>T , CM000681.2:g.38525455C>T | GRCh38 |
| NC_000019.9:g.39016095C>T , CM000681.1:g.39016095C>T | GRCh37 |
| NC_000019.8:g.43707935C>T | NCBI36 |
| NG_008866.1:g.96756C>T , LRG_766:g.96756C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.10518C>T | ENSP00000471601.2:n.10518C>T | |
| ENST00000359596.8:c.10579C>T MANE Select | ENSP00000352608.2:p.Pro3527Ser | |
| ENST00000355481.8:c.10564C>T | ENSP00000347667.3:p.Pro3522Ser | |
| ENST00000359596.7:c.10579C>T | ENSP00000352608.2:p.Pro3527Ser | |
| ENST00000360985.7:c.10561C>T | ENSP00000354254.4:p.Pro3521Ser | |
| ENST00000594335.5:c.3966C>T | ||
| ENST00000599547.5:c.1386C>T | ||
| NM_000540.2:c.10579C>T , LRG_766t1:c.10579C>T | NP_000531.2:p.Pro3527Ser | |
| NM_001042723.1:c.10564C>T | NP_001036188.1:p.Pro3522Ser | |
| XM_006723317.1:c.10579C>T | XP_006723380.1:p.Pro3527Ser | |
| XM_006723319.1:c.10564C>T | XP_006723382.1:p.Pro3522Ser | |
| XM_011527204.1:c.10576C>T | XP_011525506.1:p.Pro3526Ser | |
| XM_011527205.1:c.10579C>T | XP_011525507.1:p.Pro3527Ser | |
| XM_006723317.2:c.10579C>T | XP_006723380.1:p.Pro3527Ser | |
| XM_006723319.2:c.10564C>T | XP_006723382.1:p.Pro3522Ser | |
| XM_011527205.2:c.10579C>T | XP_011525507.1:p.Pro3527Ser | |
| NM_000540.3:c.10579C>T MANE Select | NP_000531.2:p.Pro3527Ser | |
| NM_001042723.2:c.10564C>T | NP_001036188.1:p.Pro3522Ser |