HGVS | Genome Assembly |
---|---|
NC_000020.11:g.45093159T= , CM000682.2:g.45093159T= | GRCh38 |
NC_000020.10:g.43721800T= , CM000682.1:g.43721800T= | GRCh37 |
NC_000020.9:g.43155214T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000537075.3:c.*1711A= MANE Select | ENSP00000445595.1:n.*1711A= | |
ENST00000306117.5:c.*1711A= | ENSP00000307694.1:n.*1711A= | |
NM_002251.3:c.*1711A= | NP_002242.2:n.*1711A= | |
XM_005260409.3:c.*1711A= | XP_005260466.1:n.*1711A= | |
NM_001322799.1:c.*1711A= | NP_001309728.1:n.*1711A= | |
NM_002251.4:c.*1711A= | NP_002242.2:n.*1711A= | |
XM_017027846.1:c.*1711A= | XP_016883335.1:n.*1711A= | |
NM_001322799.2:c.*1711A= MANE Select | NP_001309728.1:n.*1711A= | |
NM_002251.5:c.*1711A= | NP_002242.2:n.*1711A= |