Linked Data
MyVariant Identifiers:
chr18:g.29178617C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31598654C>G , CM000680.2:g.31598654C>G | GRCh38 |
| NC_000018.9:g.29178617C>G , CM000680.1:g.29178617C>G | GRCh37 |
| NC_000018.8:g.27432615C>G | NCBI36 |
| NG_009490.1:g.11888C>G , LRG_416:g.11888C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000237014.8:c.423C>G MANE Select | ENSP00000237014.4:p.Val141= | |
| ENST00000610404.5:c.327C>G | ENSP00000477599.2:p.Val109= | |
| ENST00000649620.1:c.423C>G | ENSP00000497927.1:p.Val141= | |
| ENST00000237014.7:c.423C>G | ENSP00000237014.3:p.Val141= | |
| ENST00000610404.4:c.537C>G | ENSP00000477599.1:p.Val179= | |
| ENST00000613781.1:c.399C>G | ENSP00000479174.1:p.Val133= | |
| NM_000371.3:c.423C>G , LRG_416t1:c.423C>G | NP_000362.1:p.Val141= | |
| NM_000371.4:c.423C>G MANE Select | NP_000362.1:p.Val141= |