HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47373519C>A , CM000664.2:g.47373519C>A | GRCh38 |
NC_000002.11:g.47600658C>A , CM000664.1:g.47600658C>A | GRCh37 |
NC_000002.10:g.47454162C>A | NCBI36 |
NG_012352.2:g.33357C>A , LRG_215:g.33357C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263735.9:c.133C>A MANE Select | ENSP00000263735.4:p.Gln45Lys | |
ENST00000263735.8:c.133C>A | ENSP00000263735.4:p.Gln45Lys | |
ENST00000405271.5:c.217C>A | ENSP00000385476.1:p.Gln73Lys | |
ENST00000419334.1:c.361C>A | ENSP00000389028.1:p.Gln121Lys | |
ENST00000456133.5:c.217C>A | ENSP00000410675.1:p.Gln73Lys | |
ENST00000474691.1:n.164C>A | ||
NM_002354.2:c.133C>A , LRG_215t1:c.133C>A | NP_002345.2:p.Gln45Lys | |
NM_002354.3:c.133C>A MANE Select | NP_002345.2:p.Gln45Lys |