Linked Data
ClinVar Variation Id:
553111
ClinVar RCV Id:
RCV000668492
dbSNP Id:
rs767543051
ExAC:
7:65547912 C / T
gnomAD v2:
7-65547912-C-T
gnomAD v3:
7-66082925-C-T
gnomAD v4:
7-66082925-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.66082925C>T , CM000669.2:g.66082925C>T | GRCh38 |
| NC_000007.13:g.65547912C>T , CM000669.1:g.65547912C>T | GRCh37 |
| NC_000007.12:g.65185347C>T | NCBI36 |
| NG_009288.1:g.12137C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000304874.14:c.337C>T MANE Select | ENSP00000307188.9:p.Arg113Trp | |
| ENST00000362000.10:c.142C>T | ENSP00000354710.6:p.Arg48Trp | |
| ENST00000380839.9:c.337C>T | ENSP00000370219.4:p.Arg113Trp | |
| ENST00000395331.4:c.337C>T | ENSP00000378740.3:p.Arg113Trp | |
| ENST00000395332.8:c.337C>T | ENSP00000378741.3:p.Arg113Trp | |
| ENST00000671817.1:c.337C>T | ENSP00000500462.1:p.Arg113Trp | |
| ENST00000672498.1:c.337C>T | ENSP00000500227.1:p.Arg113Trp | |
| ENST00000672586.1:n.242C>T | ||
| ENST00000672676.1:n.507C>T | ||
| ENST00000673149.1:n.149C>T | ||
| ENST00000673350.1:n.585C>T | ||
| ENST00000673518.1:c.337C>T | ENSP00000499889.1:p.Arg113Trp | |
| ENST00000673594.1:n.186C>T | ||
| ENST00000304874.13:c.337C>T | ENSP00000307188.9:p.Arg113Trp | |
| ENST00000362000.9:c.142C>T | ENSP00000354710.5:p.Arg48Trp | |
| ENST00000380839.8:c.337C>T | ENSP00000370219.4:p.Arg113Trp | |
| ENST00000395331.3:c.337C>T | ENSP00000378740.3:p.Arg113Trp | |
| ENST00000395332.7:c.337C>T | ENSP00000378741.3:p.Arg113Trp | |
| ENST00000487982.5:n.403C>T | ||
| ENST00000496336.1:n.578C>T | ||
| NM_000048.3:c.337C>T | NP_000039.2:p.Arg113Trp | |
| NM_001024943.1:c.337C>T | NP_001020114.1:p.Arg113Trp | |
| NM_001024944.1:c.337C>T | NP_001020115.1:p.Arg113Trp | |
| NM_001024946.1:c.337C>T | NP_001020117.1:p.Arg113Trp | |
| NM_000048.4:c.337C>T MANE Select | NP_000039.2:p.Arg113Trp | |
| NM_001024943.2:c.337C>T | NP_001020114.1:p.Arg113Trp | |
| NM_001024944.2:c.337C>T | NP_001020115.1:p.Arg113Trp | |
| NM_001024946.2:c.337C>T | NP_001020117.1:p.Arg113Trp |