HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186673759A= , CM000663.2:g.186673759A= | GRCh38 |
NC_000001.10:g.186642891A= , CM000663.1:g.186642891A= | GRCh37 |
NC_000001.9:g.184909514A= | NCBI36 |
NG_028206.2:g.11669T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367468.10:c.*594T= MANE Select | ENSP00000356438.5:n.*594T= | |
ENST00000680451.1:c.*594T= | ENSP00000506242.1:n.*594T= | |
ENST00000681605.1:c.*2081T= | ENSP00000504900.1:n.*2081T= | |
ENST00000367468.9:c.*594T= | ENSP00000356438.5:n.*594T= | |
ENST00000490885.6:n.2824T= | ||
NM_000963.3:c.*594T= | NP_000954.1:n.*594T= | |
NM_000963.4:c.*594T= MANE Select | NP_000954.1:n.*594T= |