Linked Data
ClinVar Variation Id:
14965
ClinVar RCV Id:
RCV000016105
dbSNP Id:
rs34150306
PubMed:
PMID:6192110
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5254374T>C , CM000673.2:g.5254374T>C | GRCh38 |
| NC_000011.9:g.5275604T>C , CM000673.1:g.5275604T>C | GRCh37 |
| NC_000011.8:g.5232180T>C | NCBI36 |
| NG_000007.3:g.43242A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000336906.6:c.233A>G MANE Select | ENSP00000338082.4:p.His78Arg | |
| ENST00000380252.6:c.68A>G | ENSP00000369602.2:p.His23Arg | |
| ENST00000642908.1:c.233A>G | ENSP00000495346.1:p.His78Arg | |
| ENST00000647543.1:c.233A>G | ENSP00000496470.1:p.His78Arg | |
| ENST00000336906.4:c.233A>G | ENSP00000338082.4:p.His78Arg | |
| ENST00000380252.5:c.203A>G | ENSP00000369602.1:p.His68Arg | |
| ENST00000380259.6:c.233A>G | ENSP00000369609.2:p.His78Arg | |
| ENST00000444587.1:c.*102A>G | ENSP00000488218.1:n.*102A>G | |
| ENST00000620888.4:c.233A>G | ENSP00000479637.1:p.His78Arg | |
| ENST00000624109.1:c.122T>C | ENSP00000485458.1:p.Val41Ala | |
| NM_000184.2:c.233A>G | NP_000175.1:p.His78Arg | |
| NM_000184.3:c.233A>G MANE Select | NP_000175.1:p.His78Arg |