Linked Data
ClinVar Variation Id:
5124
ClinVar RCV Id:
RCV000005431
dbSNP Id:
rs104894320
PubMed:
PMID:11007475
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.8605404A>G , CM000674.2:g.8605404A>G | GRCh38 |
| NC_000012.11:g.8758000A>G , CM000674.1:g.8758000A>G | GRCh37 |
| NC_000012.10:g.8649267A>G | NCBI36 |
| NG_011588.1:g.12443T>C , LRG_17:g.12443T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000537228.6:c.238T>C | ENSP00000445691.1:p.Trp80Arg | |
| ENST00000543081.6:c.238T>C | ENSP00000439103.2:p.Trp80Arg | |
| ENST00000544516.6:c.157-1067T>C | ENSP00000439538.2:n.157-1067T>C | |
| ENST00000545576.2:n.347T>C | ||
| ENST00000696246.1:c.223T>C | ENSP00000512504.1:p.Trp75Arg | |
| ENST00000696271.1:n.358T>C | ||
| ENST00000696272.1:c.223T>C | ENSP00000512515.1:p.Trp75Arg | |
| ENST00000696273.1:c.271T>C | ENSP00000512516.1:p.Trp91Arg | |
| ENST00000229335.11:c.238T>C MANE Select | ENSP00000229335.6:p.Trp80Arg | |
| ENST00000229335.10:c.238T>C | ENSP00000229335.6:p.Trp80Arg | |
| ENST00000537228.5:c.238T>C | ENSP00000445691.1:p.Trp80Arg | |
| ENST00000543081.5:c.234T>C | ||
| ENST00000544516.5:c.153-1067T>C | ||
| ENST00000545512.1:c.234T>C | ||
| ENST00000545576.1:n.272T>C | ||
| NM_020661.2:c.238T>C , LRG_17t1:c.238T>C | NP_065712.1:p.Trp80Arg | |
| XM_011520772.1:c.238T>C | XP_011519074.1:p.Trp80Arg | |
| XM_011520773.1:c.238T>C | XP_011519075.1:p.Trp80Arg | |
| NM_001330343.1:c.238T>C | NP_001317272.1:p.Trp80Arg | |
| NM_020661.3:c.238T>C | NP_065712.1:p.Trp80Arg | |
| XM_011520773.2:c.238T>C | XP_011519075.1:p.Trp80Arg | |
| NM_020661.4:c.238T>C MANE Select | NP_065712.1:p.Trp80Arg | |
| NM_001330343.2:c.238T>C | NP_001317272.1:p.Trp80Arg |