Linked Data
ClinVar Variation Id:
15199
ClinVar RCV Id:
RCV000016382
dbSNP Id:
rs33991059
PubMed:
PMID:6687721
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226779C>G , CM000673.2:g.5226779C>G | GRCh38 |
| NC_000011.9:g.5248009C>G , CM000673.1:g.5248009C>G | GRCh37 |
| NC_000011.8:g.5204585C>G | NCBI36 |
| NG_000007.3:g.70837G>C | |
| NG_059281.1:g.5293G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.113G>C | ENSP00000494175.1:p.Trp38Ser | |
| ENST00000335295.4:c.113G>C MANE Select | ENSP00000333994.3:p.Trp38Ser | |
| ENST00000380315.2:c.113G>C | ENSP00000369671.2:p.Trp38Ser | |
| ENST00000475226.1:n.45G>C | ||
| ENST00000485743.1:n.164G>C | ||
| ENST00000633227.1:c.97G>C | ENSP00000488004.1:p.Gly33Arg | |
| NM_000518.4:c.113G>C | NP_000509.1:p.Trp38Ser | |
| NM_000518.5:c.113G>C MANE Select | NP_000509.1:p.Trp38Ser |