HGVS | Genome Assembly |
---|---|
NC_000020.11:g.54650677T= , CM000682.2:g.54650677T= | GRCh38 |
NC_000020.10:g.53267216T= , CM000682.1:g.53267216T= | GRCh37 |
NC_000020.9:g.52700623T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262593.10:c.*198T= MANE Select | ENSP00000262593.5:n.*198T= | |
ENST00000262593.9:c.*198T= | ENSP00000262593.5:n.*198T= | |
ENST00000395939.5:c.*198T= | ENSP00000379270.1:n.*198T= | |
NM_018431.4:c.*198T= | NP_060901.2:n.*198T= | |
NM_177959.2:c.*198T= | NP_808874.1:n.*198T= | |
XM_011528903.1:c.*198T= | XP_011527205.1:n.*198T= | |
XM_011528904.1:c.*198T= | XP_011527206.1:n.*198T= | |
XM_024451946.1:c.*198T= | XP_024307714.1:n.*198T= | |
NM_018431.5:c.*198T= MANE Select | NP_060901.2:n.*198T= | |
NM_177959.3:c.*198T= | NP_808874.1:n.*198T= |