HGVS | Genome Assembly |
---|---|
NC_000020.11:g.54650442G= , CM000682.2:g.54650442G= | GRCh38 |
NC_000020.10:g.53266981G= , CM000682.1:g.53266981G= | GRCh37 |
NC_000020.9:g.52700388G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262593.10:c.884G= MANE Select | ENSP00000262593.5:p.Arg295= | |
ENST00000262593.9:c.884G= | ENSP00000262593.5:p.Arg295= | |
ENST00000395939.5:c.560G= | ENSP00000379270.1:p.Arg187= | |
NM_018431.4:c.884G= | NP_060901.2:p.Arg295= | |
NM_177959.2:c.560G= | NP_808874.1:p.Arg187= | |
XM_011528903.1:c.848G= | XP_011527205.1:p.Arg283= | |
XM_011528904.1:c.560G= | XP_011527206.1:p.Arg187= | |
XM_024451946.1:c.848G= | XP_024307714.1:p.Arg283= | |
NM_018431.5:c.884G= MANE Select | NP_060901.2:p.Arg295= | |
NM_177959.3:c.560G= | NP_808874.1:p.Arg187= |