HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37715793G= , CM000684.2:g.37715793G= | GRCh38 |
NC_000022.10:g.38111800G= , CM000684.1:g.38111800G= | GRCh37 |
NC_000022.9:g.36441746G= | NCBI36 |
NG_012857.1:g.23806G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000644935.1:c.487G= MANE Select | ENSP00000496394.1:p.Glu163= | |
ENST00000344404.10:c.285G= | ENSP00000340312.6:p.Arg95= | |
ENST00000406386.7:c.487G= | ENSP00000384312.3:p.Glu163= | |
ENST00000455236.4:c.1444G= | ENSP00000477208.1:n.1444G= | |
ENST00000492485.5:n.421G= | ||
NM_001039141.2:c.487G= | NP_001034230.1:p.Glu163= | |
NM_001039141.3:c.487G= MANE Select | NP_001034230.1:p.Glu163= |