Linked Data
ClinVar Variation Id:
15287
ClinVar RCV Id:
RCV000016518
dbSNP Id:
rs33974325
PubMed:
PMID:1227988
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226614T>G , CM000673.2:g.5226614T>G | GRCh38 |
| NC_000011.9:g.5247844T>G , CM000673.1:g.5247844T>G | GRCh37 |
| NC_000011.8:g.5204420T>G | NCBI36 |
| NG_000007.3:g.71002A>C | |
| NG_059281.1:g.5458A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647020.1:c.278A>C | ENSP00000494175.1:p.His93Pro | |
| ENST00000335295.4:c.278A>C MANE Select | ENSP00000333994.3:p.His93Pro | |
| ENST00000475226.1:n.210A>C | ||
| ENST00000485743.1:n.329A>C | ||
| ENST00000633227.1:c.*94A>C | ENSP00000488004.1:n.*94A>C | |
| NM_000518.4:c.278A>C | NP_000509.1:p.His93Pro | |
| NM_000518.5:c.278A>C MANE Select | NP_000509.1:p.His93Pro |