HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94007647C= , CM000663.2:g.94007647C= | GRCh38 |
NC_000001.10:g.94473203C= , CM000663.1:g.94473203C= | GRCh37 |
NC_000001.9:g.94245791C= | NCBI36 |
NG_009073.1:g.118503G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.5992G= MANE Select | ENSP00000359245.3:p.Val1998= | |
ENST00000370225.3:c.5992G= | ENSP00000359245.3:p.Val1998= | |
ENST00000465352.1:n.408G= | ||
ENST00000484388.1:n.106G= | ||
ENST00000536513.5:c.2368G= | ENSP00000439707.2:p.Val790= | |
NM_000350.2:c.5992G= | NP_000341.2:p.Val1998= | |
NM_000350.3:c.5992G= MANE Select | NP_000341.2:p.Val1998= |