HGVS | Genome Assembly |
---|---|
NC_000012.12:g.47973102C>T , CM000674.2:g.47973102C>T | GRCh38 |
NC_000012.11:g.48366885C>T , CM000674.1:g.48366885C>T | GRCh37 |
NC_000012.10:g.46653152C>T | NCBI36 |
NG_008072.1:g.36401G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380518.8:c.*305G>A MANE Select | ENSP00000369889.3:n.*305G>A | |
ENST00000380518.7:c.*305G>A | ENSP00000369889.3:n.*305G>A | |
NM_001844.4:c.*305G>A | NP_001835.3:n.*305G>A | |
NM_033150.2:c.*305G>A | NP_149162.2:n.*305G>A | |
XM_006719242.2:c.*305G>A | XP_006719305.2:n.*305G>A | |
XM_011537928.1:c.*305G>A | XP_011536230.1:n.*305G>A | |
XM_011537929.1:c.*305G>A | XP_011536231.1:n.*305G>A | |
XM_011537930.1:c.*305G>A | XP_011536232.1:n.*305G>A | |
XM_011537931.1:c.*305G>A | XP_011536233.1:n.*305G>A | |
XM_011537932.1:c.*305G>A | XP_011536234.1:n.*305G>A | |
XM_011537933.1:c.*305G>A | XP_011536235.1:n.*305G>A | |
XM_011537934.1:c.*305G>A | XP_011536236.1:n.*305G>A | |
XM_011537935.1:c.*305G>A | XP_011536237.1:n.*305G>A | |
XM_017018828.1:c.*305G>A | XP_016874317.1:n.*305G>A | |
XM_017018829.1:c.*305G>A | XP_016874318.1:n.*305G>A | |
XM_017018830.1:c.*305G>A | XP_016874319.1:n.*305G>A | |
XM_017018831.2:c.*305G>A | XP_016874320.1:n.*305G>A | |
NM_001844.5:c.*305G>A MANE Select | NP_001835.3:n.*305G>A | |
NM_033150.3:c.*305G>A | NP_149162.2:n.*305G>A |