Linked Data
ClinVar Variation Id:
1568530
ClinVar RCV Id:
RCV002217116
dbSNP Id:
rs2136355353
MyVariant Identifiers:
chr12:g.12870788A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717854A>G , CM000674.2:g.12717854A>G | GRCh38 |
| NC_000012.11:g.12870788A>G , CM000674.1:g.12870788A>G | GRCh37 |
| NC_000012.10:g.12762055A>G | NCBI36 |
| NG_016341.1:g.5487A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.15A>G | ENSP00000507272.1:p.Arg5= | |
| ENST00000682620.1:n.1631-971A>G | ||
| ENST00000684771.1:n.585-971A>G | ||
| ENST00000228872.9:c.15A>G MANE Select | ENSP00000228872.4:p.Arg5= | |
| ENST00000228872.8:c.15A>G | ENSP00000228872.4:p.Arg5= | |
| ENST00000396340.1:c.15A>G | ENSP00000379629.1:p.Arg5= | |
| ENST00000477087.1:n.155-971A>G | ||
| NM_004064.4:c.15A>G | NP_004055.1:p.Arg5= | |
| NM_004064.5:c.15A>G MANE Select | NP_004055.1:p.Arg5= |