Linked Data
ClinVar Variation Id:
1489478
ClinVar RCV Id:
RCV001978315
dbSNP Id:
rs138310841
gnomAD v3:
7-66082919-C-T
gnomAD v4:
7-66082919-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.66082919C>T , CM000669.2:g.66082919C>T | GRCh38 |
| NC_000007.13:g.65547906C>T , CM000669.1:g.65547906C>T | GRCh37 |
| NC_000007.12:g.65185341C>T | NCBI36 |
| NG_009288.1:g.12131C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000304874.14:c.331C>T MANE Select | ENSP00000307188.9:p.Arg111Trp | |
| ENST00000362000.10:c.136C>T | ENSP00000354710.6:p.Arg46Trp | |
| ENST00000380839.9:c.331C>T | ENSP00000370219.4:p.Arg111Trp | |
| ENST00000395331.4:c.331C>T | ENSP00000378740.3:p.Arg111Trp | |
| ENST00000395332.8:c.331C>T | ENSP00000378741.3:p.Arg111Trp | |
| ENST00000671817.1:c.331C>T | ENSP00000500462.1:p.Arg111Trp | |
| ENST00000672498.1:c.331C>T | ENSP00000500227.1:p.Arg111Trp | |
| ENST00000672586.1:n.236C>T | ||
| ENST00000672676.1:n.501C>T | ||
| ENST00000673149.1:n.143C>T | ||
| ENST00000673350.1:n.579C>T | ||
| ENST00000673518.1:c.331C>T | ENSP00000499889.1:p.Arg111Trp | |
| ENST00000673594.1:n.180C>T | ||
| ENST00000304874.13:c.331C>T | ENSP00000307188.9:p.Arg111Trp | |
| ENST00000362000.9:c.136C>T | ENSP00000354710.5:p.Arg46Trp | |
| ENST00000380839.8:c.331C>T | ENSP00000370219.4:p.Arg111Trp | |
| ENST00000395331.3:c.331C>T | ENSP00000378740.3:p.Arg111Trp | |
| ENST00000395332.7:c.331C>T | ENSP00000378741.3:p.Arg111Trp | |
| ENST00000487982.5:n.397C>T | ||
| ENST00000496336.1:n.572C>T | ||
| NM_000048.3:c.331C>T | NP_000039.2:p.Arg111Trp | |
| NM_001024943.1:c.331C>T | NP_001020114.1:p.Arg111Trp | |
| NM_001024944.1:c.331C>T | NP_001020115.1:p.Arg111Trp | |
| NM_001024946.1:c.331C>T | NP_001020117.1:p.Arg111Trp | |
| NM_000048.4:c.331C>T MANE Select | NP_000039.2:p.Arg111Trp | |
| NM_001024943.2:c.331C>T | NP_001020114.1:p.Arg111Trp | |
| NM_001024944.2:c.331C>T | NP_001020115.1:p.Arg111Trp | |
| NM_001024946.2:c.331C>T | NP_001020117.1:p.Arg111Trp |