HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312854C>A , CM000673.2:g.118312854C>A | GRCh38 |
NC_000011.9:g.118183569C>A , CM000673.1:g.118183569C>A | GRCh37 |
NC_000011.8:g.117688779C>A | NCBI36 |
NG_007383.1:g.13275C>A , LRG_38:g.13275C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.340C>A MANE Select | ENSP00000354566.4:p.Leu114Met | |
ENST00000361763.8:c.340C>A | ENSP00000354566.4:p.Leu114Met | |
ENST00000526146.5:n.886C>A | ||
ENST00000528435.5:n.893C>A | ||
ENST00000528600.1:c.322C>A | ENSP00000433975.1:p.Leu108Met | |
ENST00000529713.5:n.446C>A | ||
ENST00000531913.1:n.711C>A | ||
NM_000733.3:c.340C>A , LRG_38t1:c.340C>A | NP_000724.1:p.Leu114Met | |
NM_000733.4:c.340C>A MANE Select | NP_000724.1:p.Leu114Met |