Linked Data
ClinVar Variation Id:
446846
dbSNP Id:
rs146682319
ExAC:
7:4820890 C / T
gnomAD v2:
7-4820890-C-T
gnomAD v3:
7-4781259-C-T
gnomAD v4:
7-4781259-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.4781259C>T , CM000669.2:g.4781259C>T | GRCh38 |
| NC_000007.13:g.4820890C>T , CM000669.1:g.4820890C>T | GRCh37 |
| NC_000007.12:g.4787416C>T | NCBI36 |
| NG_028111.1:g.10629C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000477680.6:n.125-2057C>T | ||
| ENST00000647984.1:c.126C>T | ENSP00000497794.1:p.Leu42= | |
| ENST00000648925.1:c.126C>T | ENSP00000496830.1:p.Leu42= | |
| ENST00000649063.2:c.126C>T MANE Select | ENSP00000497815.1:p.Leu42= | |
| ENST00000650310.1:c.126C>T | ENSP00000497395.1:p.Leu42= | |
| ENST00000650451.1:c.126C>T | ENSP00000496998.1:p.Leu42= | |
| ENST00000348624.4:c.126C>T | ENSP00000297562.4:p.Leu42= | |
| ENST00000477680.5:n.125-2057C>T | ||
| ENST00000496303.5:n.190C>T | ||
| NM_014855.2:c.126C>T | NP_055670.1:p.Leu42= | |
| XR_242109.1:n.151C>T | ||
| NM_001364858.1:c.-156C>T | NP_001351787.1:n.-156C>T | |
| NM_014855.3:c.126C>T MANE Select | NP_055670.1:p.Leu42= | |
| NR_157345.1:n.219C>T |