Linked Data
ClinVar Variation Id:
360323
ClinVar RCV Id:
RCV000396245
dbSNP Id:
rs886062353
gnomAD v2:
7-4825302-C-T
gnomAD v3:
7-4785671-C-T
gnomAD v4:
7-4785671-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.4785671C>T , CM000669.2:g.4785671C>T | GRCh38 |
| NC_000007.13:g.4825302C>T , CM000669.1:g.4825302C>T | GRCh37 |
| NC_000007.12:g.4791828C>T | NCBI36 |
| NG_028111.1:g.15041C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000477680.6:n.877C>T | ||
| ENST00000496303.6:n.947C>T | ||
| ENST00000647628.1:n.610C>T | ||
| ENST00000647984.1:c.*464C>T | ENSP00000497794.1:n.*464C>T | |
| ENST00000648925.1:c.1119C>T | ENSP00000496830.1:p.Phe373= | |
| ENST00000649063.2:c.1119C>T MANE Select | ENSP00000497815.1:p.Phe373= | |
| ENST00000649315.1:c.329C>T | ||
| ENST00000649419.1:n.395C>T | ||
| ENST00000650310.1:c.1119C>T | ENSP00000497395.1:p.Phe373= | |
| ENST00000348624.4:c.1119C>T | ENSP00000297562.4:p.Phe373= | |
| ENST00000477680.5:n.877C>T | ||
| ENST00000496303.5:n.1183C>T | ||
| NM_014855.2:c.1119C>T | NP_055670.1:p.Phe373= | |
| XR_242109.1:n.1144C>T | ||
| NM_001364858.1:c.651C>T | NP_001351787.1:p.Phe217= | |
| NM_014855.3:c.1119C>T MANE Select | NP_055670.1:p.Phe373= | |
| NR_157345.1:n.1212C>T |