HGVS | Genome Assembly |
---|---|
NC_000007.14:g.150992732C= , CM000669.2:g.150992732C= | GRCh38 |
NC_000007.13:g.150689820C= , CM000669.1:g.150689820C= | GRCh37 |
NC_000007.12:g.150320753C= | NCBI36 |
NG_011992.1:g.6674C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297494.8:c.-51-1021C= MANE Select | ENSP00000297494.3:n.-51-1021C= | |
ENST00000297494.7:c.-51-1021C= | ENSP00000297494.3:n.-51-1021C= | |
ENST00000461406.5:c.-149+1432C= | ENSP00000417143.1:n.-149+1432C= | |
NM_000603.4:c.-51-1021C= | NP_000594.2:n.-51-1021C= | |
NM_000603.5:c.-51-1021C= MANE Select | NP_000594.2:n.-51-1021C= |