HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43169276C= , CM000683.2:g.43169276C= | GRCh38 |
NG_009823.1:g.5246C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291554.6:c.177C= MANE Select | ENSP00000291554.2:p.Ser59= | |
ENST00000482775.1:n.190C= | ||
NM_000394.3:c.177C= | NP_000385.1:p.Ser59= | |
XR_001755073.1:n.647+1761G= | ||
NM_000394.4:c.177C= MANE Select | NP_000385.1:p.Ser59= |