HGVS | Genome Assembly |
---|---|
NC_000005.10:g.70049684C= , CM000667.2:g.70049684C= | GRCh38 |
NC_000005.9:g.69345511C= , CM000667.1:g.69345511C= | GRCh37 |
NC_000005.8:g.69381267C= | NCBI36 |
NG_008728.1:g.5162C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380743.9:c.-2C= MANE Select | ENSP00000370119.4:n.-2C= | |
ENST00000380742.8:c.-2C= | ENSP00000370118.4:n.-2C= | |
ENST00000380743.8:c.-2C= | ENSP00000370119.4:n.-2C= | |
ENST00000506734.5:c.-2C= | ENSP00000424799.1:n.-2C= | |
ENST00000511812.5:c.-2C= | ENSP00000424282.1:n.-2C= | |
ENST00000626847.2:c.-2C= | ENSP00000486152.1:n.-2C= | |
NM_017411.3:c.-2C= | NP_059107.1:n.-2C= | |
NM_022875.2:c.-2C= | NP_075013.1:n.-2C= | |
NM_022876.2:c.-2C= | NP_075014.1:n.-2C= | |
NM_022877.2:c.-2C= | NP_075015.1:n.-2C= | |
XM_011543599.1:c.-2C= | XP_011541901.1:n.-2C= | |
XM_011543600.1:c.-2C= | XP_011541902.1:n.-2C= | |
XM_011543601.1:c.-2C= | XP_011541903.1:n.-2C= | |
XM_011543602.1:c.-2C= | XP_011541904.1:n.-2C= | |
XM_011543603.1:c.-2C= | XP_011541905.1:n.-2C= | |
XR_948432.1:n.1054+61680C= | ||
XM_011543600.2:c.-2C= | XP_011541902.1:n.-2C= | |
XM_011543602.3:c.-2C= | XP_011541904.1:n.-2C= | |
XM_011543603.3:c.-2C= | XP_011541905.1:n.-2C= | |
XM_017009787.1:c.-2C= | XP_016865276.1:n.-2C= | |
NM_017411.4:c.-2C= MANE Select | NP_059107.1:n.-2C= | |
NM_022875.3:c.-2C= | NP_075013.1:n.-2C= |