HGVS | Genome Assembly |
---|---|
NC_000015.10:g.84840525A>G , CM000677.2:g.84840525A>G | GRCh38 |
NC_000015.9:g.85383756A>G , CM000677.1:g.85383756A>G | GRCh37 |
NC_000015.8:g.83184760A>G | NCBI36 |
NG_054748.1:g.28895A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258888.6:c.1246A>G MANE Select | ENSP00000258888.6:p.Lys416Glu | |
ENST00000258888.5:c.1852A>G | ENSP00000258888.5:p.Lys618Glu | |
NM_020778.4:c.1852A>G | NP_065829.3:p.Lys618Glu | |
NM_020778.5:c.1246A>G MANE Select | NP_065829.4:p.Lys416Glu |