HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149981044G= , CM000667.2:g.149981044G= | GRCh38 |
NC_000005.9:g.149360607G= , CM000667.1:g.149360607G= | GRCh37 |
NC_000005.8:g.149340800G= | NCBI36 |
NG_007147.2:g.22162G= , LRG_684:g.22162G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.1451G= MANE Select | ENSP00000286298.4:p.Gly484= | |
ENST00000286298.4:c.1451G= | ENSP00000286298.4:p.Gly484= | |
ENST00000503336.1:c.372+2693G= | ENSP00000426053.1:n.372+2693G= | |
NM_000112.3:c.1451G= , LRG_684t1:c.1451G= | NP_000103.2:p.Gly484= | |
XM_017009191.2:c.1451G= | XP_016864680.1:p.Gly484= | |
NM_000112.4:c.1451G= MANE Select | NP_000103.2:p.Gly484= |