HGVS | Genome Assembly |
---|---|
NC_000008.11:g.16992926T= , CM000670.2:g.16992926T= | GRCh38 |
NC_000008.10:g.16850435T= , CM000670.1:g.16850435T= | GRCh37 |
NC_000008.9:g.16894806T= | NCBI36 |
NG_015978.1:g.14240A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000180166.6:c.*146A= MANE Select | ENSP00000180166.5:n.*146A= | |
ENST00000180166.5:c.*146A= | ENSP00000180166.5:n.*146A= | |
NM_019851.2:c.*146A= | NP_062825.1:n.*146A= | |
NM_019851.3:c.*146A= MANE Select | NP_062825.1:n.*146A= |