HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6319442C>A , CM000673.2:g.6319442C>A | GRCh38 |
NC_000011.9:g.6340672C>A , CM000673.1:g.6340672C>A | GRCh37 |
NC_000011.8:g.6297248C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303927.4:c.507G>T MANE Select | ENSP00000307292.3:p.Glu169Asp | |
ENST00000303927.3:c.507G>T | ENSP00000307292.3:p.Glu169Asp | |
ENST00000524852.1:n.293G>T | ||
ENST00000530979.1:c.603G>T | ENSP00000432047.1:p.Glu201Asp | |
ENST00000532354.1:n.529G>T | ||
NM_145040.2:c.507G>T | NP_659477.2:p.Glu169Asp | |
XR_930997.1:n.720+1222C>A | ||
XR_001748106.1:n.53C>A | ||
XR_242848.4:n.302C>A | ||
NM_145040.3:c.507G>T MANE Select | NP_659477.2:p.Glu169Asp |