HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50489815G= , CM000684.2:g.50489815G= | GRCh38 |
NC_000022.10:g.50928244G= , CM000684.1:g.50928244G= | GRCh37 |
NC_000022.9:g.49275110G= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216075.11:c.817G= MANE Select | ENSP00000216075.6:p.Gly273= | |
ENST00000216075.10:c.817G= | ENSP00000216075.6:p.Gly273= | |
ENST00000395732.7:c.803G= | ENSP00000379081.3:p.Gly268= | |
ENST00000395733.7:c.686G= | ENSP00000379082.3:p.Gly229= | |
ENST00000451761.1:c.757G= | ENSP00000409894.1:p.Gly253= | |
NM_017584.5:c.817G= | NP_060054.4:p.Gly273= | |
XM_005261925.3:c.679G= | XP_005261982.1:p.Gly227= | |
XR_244455.2:n.3313G= | ||
XM_005261925.4:c.679G= | XP_005261982.1:p.Gly227= | |
NM_017584.6:c.817G= MANE Select | NP_060054.4:p.Gly273= |