Linked Data
ClinVar Variation Id:
24832
ClinVar RCV Id:
RCV000421390
RCV000431203
RCV000419206
RCV000441473
RCV000434006
RCV000439037
RCV000423753
RCV000520995
RCV000431590
RCV000635423
RCV000763030
RCV002316201
RCV004018654
dbSNP Id:
rs377767347
COSMIC:
COSM14122
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.51065549G>A , CM000680.2:g.51065549G>A | GRCh38 |
| NC_000018.9:g.48591919G>A , CM000680.1:g.48591919G>A | GRCh37 |
| NC_000018.8:g.46845917G>A | NCBI36 |
| NG_013013.2:g.102510G>A , LRG_318:g.102510G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000588860.6:c.1082G>A | ENSP00000465878.2:p.Arg361His | |
| ENST00000589076.6:c.1082G>A | ENSP00000466934.2:p.Arg361His | |
| ENST00000589941.2:c.1082G>A | ENSP00000465874.2:p.Arg361His | |
| ENST00000590061.2:c.1082G>A | ENSP00000464772.2:p.Arg361His | |
| ENST00000593223.2:c.1082G>A | ENSP00000466118.2:p.Arg361His | |
| ENST00000611848.2:c.1082G>A | ENSP00000478613.2:p.Arg361His | |
| ENST00000684953.1:n.2454G>A | ||
| ENST00000685090.1:n.1533G>A | ||
| ENST00000685232.1:n.1190G>A | ||
| ENST00000688307.1:n.333G>A | ||
| ENST00000688574.1:n.1190G>A | ||
| ENST00000688903.1:n.1296G>A | ||
| ENST00000691124.1:n.2564G>A | ||
| ENST00000342988.8:c.1082G>A MANE Select | ENSP00000341551.3:p.Arg361His | |
| ENST00000342988.7:c.1082G>A | ENSP00000341551.3:p.Arg361His | |
| ENST00000398417.6:c.1082G>A | ENSP00000381452.1:p.Arg361His | |
| ENST00000588745.5:c.794G>A | ENSP00000464901.1:p.Arg265His | |
| ENST00000591126.5:n.3083G>A | ||
| ENST00000592186.5:c.955+5633G>A | ENSP00000468611.1:n.955+5633G>A | |
| ENST00000611848.1:c.282G>A | ||
| NM_005359.5:c.1082G>A , LRG_318t1:c.1082G>A | NP_005350.1:p.Arg361His | |
| NM_005359.6:c.1082G>A MANE Select | NP_005350.1:p.Arg361His |