Linked Data
ClinVar Variation Id:
65838
dbSNP Id:
rs573951598
ExAC:
2:219679131 C / T
gnomAD v2:
2-219679131-C-T
gnomAD v3:
2-218814408-C-T
gnomAD v4:
2-218814408-C-T
COSMIC:
COSM4933266
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814408C>T , CM000664.2:g.218814408C>T | GRCh38 |
| NC_000002.11:g.219679131C>T , CM000664.1:g.219679131C>T | GRCh37 |
| NC_000002.10:g.219387375C>T | NCBI36 |
| NG_007959.1:g.37660C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.1213C>T MANE Select | ENSP00000258415.4:p.Arg405Trp | |
| ENST00000258415.8:c.1213C>T | ENSP00000258415.4:p.Arg405Trp | |
| ENST00000494263.5:n.1839C>T | ||
| NM_000784.3:c.1213C>T | NP_000775.1:p.Arg405Trp | |
| XM_017003488.2:c.793C>T | XP_016858977.1:p.Arg265Trp | |
| NM_000784.4:c.1213C>T MANE Select | NP_000775.1:p.Arg405Trp |