HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44287118G= , CM000683.2:g.44287118G= | GRCh38 |
NC_000021.8:g.45707001G= , CM000683.1:g.45707001G= | GRCh37 |
NC_000021.7:g.44531429G= | NCBI36 |
NG_009556.1:g.6239G= , LRG_18:g.6239G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291582.6:c.448G= MANE Select | ENSP00000291582.5:p.Gly150= | |
ENST00000291582.5:c.448G= | ENSP00000291582.5:p.Gly150= | |
ENST00000527919.5:n.609G= | ||
ENST00000530812.5:n.617G= | ||
NM_000383.3:c.448G= | NP_000374.1:p.Gly150= | |
XM_011529551.1:c.448G= | XP_011527853.1:p.Gly150= | |
NM_000383.4:c.448G= MANE Select | NP_000374.1:p.Gly150= |