HGVS | Genome Assembly |
---|---|
NC_000019.10:g.8580892C= , CM000681.2:g.8580892C= | GRCh38 |
NC_000019.9:g.8645776C= , CM000681.1:g.8645776C= | GRCh37 |
NC_000019.8:g.8551776C= | NCBI36 |
NG_011840.2:g.34811G= | |
NG_052844.1:g.1556G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000597188.6:c.*1G= MANE Select | ENSP00000471851.1:n.*1G= | |
ENST00000270328.8:c.*1G= | ENSP00000270328.4:n.*1G= | |
ENST00000593913.5:c.*2190G= | ENSP00000469901.1:n.*2190G= | |
ENST00000595838.5:c.*1G= | ENSP00000470501.1:n.*1G= | |
ENST00000597188.5:c.*1G= | ENSP00000471851.1:n.*1G= | |
NM_001282352.1:c.*1G= | NP_001269281.1:n.*1G= | |
NM_030957.3:c.*1G= | NP_112219.3:n.*1G= | |
XM_006722917.2:c.*1G= | XP_006722980.1:n.*1G= | |
XM_011528331.1:c.*1G= | XP_011526633.1:n.*1G= | |
XM_011528332.1:c.*1G= | XP_011526634.1:n.*1G= | |
XM_011528333.1:c.*1G= | XP_011526635.1:n.*1G= | |
XM_011528334.1:c.*1G= | XP_011526636.1:n.*1G= | |
XM_011528335.1:c.*1G= | XP_011526637.1:n.*1G= | |
XM_011528336.1:c.*1G= | XP_011526638.1:n.*1G= | |
XM_006722917.3:c.*1G= | XP_006722980.1:n.*1G= | |
XM_017027338.2:c.*1G= | XP_016882827.1:n.*1G= | |
XM_017027339.1:c.*1G= | XP_016882828.1:n.*1G= | |
XM_017027340.1:c.*1G= | XP_016882829.1:n.*1G= | |
NM_030957.4:c.*1G= MANE Select | NP_112219.3:n.*1G= | |
NM_001282352.2:c.*1G= | NP_001269281.1:n.*1G= |