HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31595177A>G , CM000680.2:g.31595177A>G | GRCh38 |
NC_000018.9:g.29175140A>G , CM000680.1:g.29175140A>G | GRCh37 |
NC_000018.8:g.27429138A>G | NCBI36 |
NG_009490.1:g.8411A>G , LRG_416:g.8411A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237014.8:c.258A>G MANE Select | ENSP00000237014.4:p.Glu86= | |
ENST00000610404.5:c.162A>G | ENSP00000477599.2:p.Glu54= | |
ENST00000649620.1:c.258A>G | ENSP00000497927.1:p.Glu86= | |
ENST00000237014.7:c.258A>G | ENSP00000237014.3:p.Glu86= | |
ENST00000541025.2:n.284A>G | ||
ENST00000610404.4:c.258A>G | ENSP00000477599.1:p.Glu86= | |
ENST00000613781.1:c.258A>G | ENSP00000479174.1:p.Glu86= | |
NM_000371.3:c.258A>G , LRG_416t1:c.258A>G | NP_000362.1:p.Glu86= | |
NM_000371.4:c.258A>G MANE Select | NP_000362.1:p.Glu86= |