HGVS | Genome Assembly |
---|---|
NC_000011.10:g.111352254C>A , CM000673.2:g.111352254C>A | GRCh38 |
NC_000011.9:g.111222979C>A , CM000673.1:g.111222979C>A | GRCh37 |
NC_000011.8:g.110728189C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393067.7:c.*2007G>T | ENSP00000376786.3:n.*2007G>T | |
XM_005271593.1:c.*2007G>T | XP_005271650.1:n.*2007G>T | |
XM_005271594.3:c.*2007G>T | XP_005271651.1:n.*2007G>T | |
XM_006718859.1:c.*2007G>T | XP_006718922.1:n.*2007G>T | |
XM_005271593.2:c.*2007G>T | XP_005271650.1:n.*2007G>T | |
XM_006718860.4:c.*4162G>T | XP_006718923.1:n.*4162G>T | |
XM_017017932.1:c.*4162G>T | XP_016873421.1:n.*4162G>T |