HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942380T= , CM000672.2:g.94942380T= | GRCh38 |
NC_000010.10:g.96702137T= , CM000672.1:g.96702137T= | GRCh37 |
NC_000010.9:g.96692127T= | NCBI36 |
NG_008385.1:g.8723T= | |
NG_008385.2:g.9223T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.481+39T= MANE Select | ENSP00000260682.6:n.481+39T= | |
ENST00000643112.1:c.481+39T= | ENSP00000496202.1:n.481+39T= | |
ENST00000645207.1:n.634+39T= | ||
ENST00000260682.6:c.481+39T= | ENSP00000260682.6:n.481+39T= | |
ENST00000461906.1:n.545T= | ||
ENST00000473496.1:n.252+39T= | ||
NM_000771.3:c.481+39T= | NP_000762.2:n.481+39T= | |
NM_000771.4:c.481+39T= MANE Select | NP_000762.2:n.481+39T= |