Linked Data
ClinVar Variation Id:
1962426
ClinVar RCV Id:
RCV002726123
dbSNP Id:
rs1463929637
gnomAD v4:
6-1610787-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1610787C>T , CM000668.2:g.1610787C>T | GRCh38 |
| NC_000006.11:g.1611022C>T , CM000668.1:g.1611022C>T | GRCh37 |
| NC_000006.10:g.1556021C>T | NCBI36 |
| NG_009368.1:g.5342C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.342C>T MANE Select | ENSP00000493906.1:p.Phe114= | |
| ENST00000380874.3:c.342C>T | ENSP00000370256.2:p.Phe114= | |
| NM_001453.2:c.342C>T | NP_001444.2:p.Phe114= | |
| NM_001453.3:c.342C>T MANE Select | NP_001444.2:p.Phe114= |