Linked Data
ClinVar Variation Id:
18067
ClinVar RCV Id:
RCV000019690
dbSNP Id:
rs104893677
gnomAD v3:
3-148741880-C-T
gnomAD v4:
3-148741880-C-T
PubMed:
PMID:16116425
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.148741880C>T , CM000665.2:g.148741880C>T | GRCh38 |
| NC_000003.11:g.148459667C>T , CM000665.1:g.148459667C>T | GRCh37 |
| NC_000003.10:g.149942357C>T | NCBI36 |
| NG_008468.1:g.49010C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000349243.8:c.845C>T MANE Select | ENSP00000273430.3:p.Thr282Met | |
| ENST00000402260.2:c.845C>T | ENSP00000385641.3:p.Thr282Met | |
| ENST00000418473.7:c.845C>T | ENSP00000398832.4:p.Thr282Met | |
| ENST00000349243.7:c.845C>T | ENSP00000273430.3:p.Thr282Met | |
| ENST00000402260.1:c.932C>T | ENSP00000385641.2:p.Thr311Met | |
| ENST00000404754.2:c.845C>T | ENSP00000385612.2:p.Thr282Met | |
| ENST00000418473.6:c.950C>T | ENSP00000398832.3:p.Thr317Met | |
| ENST00000461609.1:c.845C>T | ENSP00000418851.1:p.Thr282Met | |
| ENST00000474935.5:c.845C>T | ENSP00000418084.1:p.Thr282Met | |
| ENST00000475347.5:c.845C>T | ENSP00000419783.1:p.Thr282Met | |
| ENST00000497524.5:c.845C>T | ENSP00000419422.1:p.Thr282Met | |
| NM_000685.4:c.845C>T | NP_000676.1:p.Thr282Met | |
| NM_004835.4:c.950C>T | NP_004826.5:p.Thr317Met | |
| NM_009585.3:c.845C>T | NP_033611.1:p.Thr282Met | |
| NM_031850.3:c.950C>T | NP_114038.4:p.Thr317Met | |
| NM_032049.3:c.932C>T | NP_114438.2:p.Thr311Met | |
| NM_000685.5:c.845C>T MANE Select | NP_000676.1:p.Thr282Met | |
| NM_001382736.1:c.845C>T | NP_001369665.1:p.Thr282Met | |
| NM_001382737.1:c.845C>T | NP_001369666.1:p.Thr282Met | |
| NM_004835.5:c.845C>T | NP_004826.6:p.Thr282Met | |
| NM_009585.4:c.845C>T | NP_033611.1:p.Thr282Met | |
| NM_031850.4:c.845C>T | NP_114038.5:p.Thr282Met | |
| NM_032049.4:c.845C>T | NP_114438.3:p.Thr282Met |