Linked Data
ClinVar Variation Id:
1023633
ClinVar RCV Id:
RCV001323714
dbSNP Id:
rs758815329
ExAC:
1:160100269 C / T
gnomAD v2:
1-160100269-C-T
gnomAD v3:
1-160130479-C-T
gnomAD v4:
1-160130479-C-T
COSMIC:
COSM898177
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160130479C>T , CM000663.2:g.160130479C>T | GRCh38 |
| NC_000001.10:g.160100269C>T , CM000663.1:g.160100269C>T | GRCh37 |
| NC_000001.9:g.158366893C>T | NCBI36 |
| NG_008014.1:g.19722C>T , LRG_6:g.19722C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.1709C>T MANE Select | ENSP00000354490.3:p.Thr570Met | |
| ENST00000361216.7:c.1709C>T | ENSP00000354490.3:p.Thr570Met | |
| ENST00000392233.7:c.1709C>T | ENSP00000376066.3:p.Thr570Met | |
| ENST00000447527.1:c.841C>T | ||
| ENST00000472488.5:n.1812C>T | ||
| NM_000702.3:c.1709C>T | NP_000693.1:p.Thr570Met | |
| NM_000702.4:c.1709C>T MANE Select | NP_000693.1:p.Thr570Met |