HGVS | Genome Assembly |
---|---|
NC_000001.11:g.119759967A= , CM000663.2:g.119759967A= | GRCh38 |
NC_000001.10:g.120302590A= , CM000663.1:g.120302590A= | GRCh37 |
NC_000001.9:g.120104113A= | NCBI36 |
NG_013348.1:g.13966T= , LRG_447:g.13966T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369406.8:c.582T= MANE Select | ENSP00000358414.3:p.Cys194= | |
ENST00000369406.7:c.582T= | ENSP00000358414.3:p.Cys194= | |
ENST00000476640.1:n.478T= | ||
ENST00000544913.2:c.560-685T= | ENSP00000439495.2:n.560-685T= | |
NM_001166107.1:c.560-685T= , LRG_447t2:c.560-685T= | NP_001159579.1:n.560-685T= | |
NM_005518.3:c.582T= , LRG_447t1:c.582T= | NP_005509.1:p.Cys194= | |
XM_011541313.1:c.582T= | XP_011539615.1:p.Cys194= | |
XM_011541313.2:c.582T= | XP_011539615.1:p.Cys194= | |
NM_005518.4:c.582T= MANE Select | NP_005509.1:p.Cys194= |