Linked Data
ClinVar Variation Id:
417162
dbSNP Id:
rs192441133
ExAC:
7:4825245 C / T
gnomAD v2:
7-4825245-C-T
gnomAD v3:
7-4785614-C-T
gnomAD v4:
7-4785614-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.4785614C>T , CM000669.2:g.4785614C>T | GRCh38 |
| NC_000007.13:g.4825245C>T , CM000669.1:g.4825245C>T | GRCh37 |
| NC_000007.12:g.4791771C>T | NCBI36 |
| NG_028111.1:g.14984C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000477680.6:n.820C>T | ||
| ENST00000496303.6:n.890C>T | ||
| ENST00000647628.1:n.553C>T | ||
| ENST00000647984.1:c.*407C>T | ENSP00000497794.1:n.*407C>T | |
| ENST00000648925.1:c.1062C>T | ENSP00000496830.1:p.His354= | |
| ENST00000649063.2:c.1062C>T MANE Select | ENSP00000497815.1:p.His354= | |
| ENST00000649315.1:c.272C>T | ||
| ENST00000649419.1:n.338C>T | ||
| ENST00000650310.1:c.1062C>T | ENSP00000497395.1:p.His354= | |
| ENST00000348624.4:c.1062C>T | ENSP00000297562.4:p.His354= | |
| ENST00000477680.5:n.820C>T | ||
| ENST00000496303.5:n.1126C>T | ||
| NM_014855.2:c.1062C>T | NP_055670.1:p.His354= | |
| XR_242109.1:n.1087C>T | ||
| NM_001364858.1:c.594C>T | NP_001351787.1:p.His198= | |
| NM_014855.3:c.1062C>T MANE Select | NP_055670.1:p.His354= | |
| NR_157345.1:n.1155C>T |