HGVS | Genome Assembly |
---|---|
NC_000013.11:g.24882851T= , CM000675.2:g.24882851T= | GRCh38 |
NC_000013.10:g.25456989T= , CM000675.1:g.25456989T= | GRCh37 |
NC_000013.9:g.24354989T= | NCBI36 |
NG_009165.2:g.45097A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381884.9:c.*326A= (CENPJ) MANE Select | ENSP00000371308.4:n.*326A= | |
ENST00000616936.4:c.*997A= (CENPJ) | ENSP00000477511.1:n.*997A= | |
NM_018451.4:c.*326A= (CENPJ) | NP_060921.3:n.*326A= | |
NR_047594.1:n.4655A= (CENPJ) | ||
NR_047595.1:n.4453A= (CENPJ) | ||
XM_011535156.1:c.*10+3556T= (RNF17) | XP_011533458.1:n.*10+3556T= | |
XM_011535156.2:c.*10+3556T= (RNF17) | XP_011533458.1:n.*10+3556T= | |
NM_018451.5:c.*326A= (CENPJ) MANE Select | NP_060921.3:n.*326A= | |
NR_047594.2:n.4627A= (CENPJ) | ||
NR_047595.2:n.4425A= (CENPJ) |