HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94989072T= , CM000672.2:g.94989072T= | GRCh38 |
NC_000010.10:g.96748829T= , CM000672.1:g.96748829T= | GRCh37 |
NC_000010.9:g.96738819T= | NCBI36 |
NG_008385.1:g.55415T= | |
NG_008385.2:g.55915T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.*44T= MANE Select | ENSP00000260682.6:n.*44T= | |
ENST00000643112.1:c.*526T= | ENSP00000496202.1:n.*526T= | |
ENST00000260682.6:c.*44T= | ENSP00000260682.6:n.*44T= | |
NM_000771.3:c.*44T= | NP_000762.2:n.*44T= | |
NM_000771.4:c.*44T= MANE Select | NP_000762.2:n.*44T= |