HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48045770C>A , CM000675.2:g.48045770C>A | GRCh38 |
NC_000013.10:g.48619906C>A , CM000675.1:g.48619906C>A | GRCh37 |
NC_000013.9:g.47517907C>A | NCBI36 |
NG_047021.1:g.13204C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258662.3:c.466C>A MANE Select | ENSP00000258662.1:p.Leu156Met | |
ENST00000258662.2:c.466C>A | ENSP00000258662.1:p.Leu156Met | |
NM_018283.2:c.466C>A | NP_060753.1:p.Leu156Met | |
NM_018283.3:c.466C>A | NP_060753.1:p.Leu156Met | |
NR_136687.1:n.646C>A | ||
NR_136688.1:n.646C>A | ||
NM_018283.4:c.466C>A MANE Select | NP_060753.1:p.Leu156Met | |
NR_136687.2:n.487C>A | ||
NR_136688.2:n.487C>A |