HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31598636C>G , CM000680.2:g.31598636C>G | GRCh38 |
NC_000018.9:g.29178599C>G , CM000680.1:g.29178599C>G | GRCh37 |
NC_000018.8:g.27432597C>G | NCBI36 |
NG_009490.1:g.11870C>G , LRG_416:g.11870C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000237014.8:c.405C>G MANE Select | ENSP00000237014.4:p.Ser135= | |
ENST00000610404.5:c.309C>G | ENSP00000477599.2:p.Ser103= | |
ENST00000649620.1:c.405C>G | ENSP00000497927.1:p.Ser135= | |
ENST00000237014.7:c.405C>G | ENSP00000237014.3:p.Ser135= | |
ENST00000610404.4:c.519C>G | ENSP00000477599.1:p.Ser173= | |
ENST00000613781.1:c.381C>G | ENSP00000479174.1:p.Ser127= | |
NM_000371.3:c.405C>G , LRG_416t1:c.405C>G | NP_000362.1:p.Ser135= | |
NM_000371.4:c.405C>G MANE Select | NP_000362.1:p.Ser135= |