HGVS | Genome Assembly |
---|---|
NC_000020.11:g.54650506A>G , CM000682.2:g.54650506A>G | GRCh38 |
NC_000020.10:g.53267045A>G , CM000682.1:g.53267045A>G | GRCh37 |
NC_000020.9:g.52700452A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262593.10:c.*27A>G MANE Select | ENSP00000262593.5:n.*27A>G | |
ENST00000262593.9:c.*27A>G | ENSP00000262593.5:n.*27A>G | |
ENST00000395939.5:c.*27A>G | ENSP00000379270.1:n.*27A>G | |
NM_018431.4:c.*27A>G | NP_060901.2:n.*27A>G | |
NM_177959.2:c.*27A>G | NP_808874.1:n.*27A>G | |
XM_011528903.1:c.*27A>G | XP_011527205.1:n.*27A>G | |
XM_011528904.1:c.*27A>G | XP_011527206.1:n.*27A>G | |
XM_024451946.1:c.*27A>G | XP_024307714.1:n.*27A>G | |
NM_018431.5:c.*27A>G MANE Select | NP_060901.2:n.*27A>G | |
NM_177959.3:c.*27A>G | NP_808874.1:n.*27A>G |