Linked Data
ClinVar Variation Id:
582457
ClinVar RCV Id:
RCV000706530
dbSNP Id:
rs1567668570
gnomAD v4:
16-67165838-C-T
COSMIC:
COSM2994221
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67165838C>T , CM000678.2:g.67165838C>T | GRCh38 |
| NC_000016.9:g.67199741C>T , CM000678.1:g.67199741C>T | GRCh37 |
| NC_000016.8:g.65757242C>T | NCBI36 |
| NG_009294.1:g.7454C>T | |
| NG_029566.1:g.337C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000517867.2:n.635C>T | ||
| ENST00000523077.2:n.851C>T | ||
| ENST00000521374.6:c.352C>T MANE Select | ENSP00000430947.2:p.Arg118Trp | |
| ENST00000434833.6:c.352C>T | ENSP00000403219.2:p.Arg118Trp | |
| ENST00000517685.5:c.352C>T | ENSP00000428978.1:p.Arg118Trp | |
| ENST00000517729.5:c.226C>T | ENSP00000430299.1:p.Arg76Trp | |
| ENST00000521314.5:c.*99C>T | ENSP00000429580.1:n.*99C>T | |
| ENST00000521374.5:c.352C>T | ENSP00000430947.1:p.Arg118Trp | |
| ENST00000521624.5:c.352C>T | ENSP00000428161.1:p.Arg118Trp | |
| ENST00000522023.1:n.419C>T | ||
| ENST00000522295.5:c.352C>T | ENSP00000427832.1:p.Arg118Trp | |
| ENST00000522870.5:n.571C>T | ||
| ENST00000523562.5:c.352C>T | ENSP00000430631.1:p.Arg118Trp | |
| ENST00000584272.5:c.352C>T | ENSP00000463706.1:p.Arg118Trp | |
| NM_001040667.2:c.352C>T | NP_001035757.1:p.Arg118Trp | |
| NM_001538.3:c.352C>T | NP_001529.2:p.Arg118Trp | |
| NM_001040667.3:c.352C>T | NP_001035757.1:p.Arg118Trp | |
| NM_001374674.1:c.352C>T | NP_001361603.1:p.Arg118Trp | |
| NM_001374675.1:c.352C>T MANE Select | NP_001361604.1:p.Arg118Trp | |
| NM_001538.4:c.352C>T | NP_001529.2:p.Arg118Trp |