HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68429763T= , CM000663.2:g.68429763T= | GRCh38 |
NC_000001.10:g.68895446T= , CM000663.1:g.68895446T= | GRCh37 |
NC_000001.9:g.68668034T= | NCBI36 |
NG_008472.1:g.25197A= | |
NG_008472.2:g.25197A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.*13A= MANE Select | ENSP00000262340.5:n.*13A= | |
ENST00000262340.5:c.*13A= | ENSP00000262340.5:n.*13A= | |
NM_000329.2:c.*13A= | NP_000320.1:n.*13A= | |
XM_017002027.1:c.*13A= | XP_016857516.1:n.*13A= | |
NM_000329.3:c.*13A= MANE Select | NP_000320.1:n.*13A= |