HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133351857A= , CM000671.2:g.133351857A= | GRCh38 |
NC_000009.10:g.135208533A= | NCBI36 |
NG_008477.1:g.9650T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371974.8:c.*56T= MANE Select | ENSP00000361042.3:n.*56T= | |
ENST00000371974.7:c.*56T= | ENSP00000361042.3:n.*56T= | |
ENST00000615505.4:c.*56T= | ENSP00000482067.1:n.*56T= | |
NM_001280787.1:c.*56T= | NP_001267716.1:n.*56T= | |
NM_003172.3:c.*56T= | NP_003163.1:n.*56T= | |
XM_011518942.1:c.*56T= | XP_011517244.1:n.*56T= | |
NM_003172.4:c.*56T= MANE Select | NP_003163.1:n.*56T= |