HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190406A= , CM000663.2:g.204190406A= | GRCh38 |
NC_000001.10:g.204159534A= , CM000663.1:g.204159534A= | GRCh37 |
NC_000001.9:g.202426157A= | NCBI36 |
NG_032151.1:g.11086T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*78T= MANE Select | ENSP00000356162.4:n.*78T= | |
ENST00000367194.4:c.*78T= | ENSP00000356162.4:n.*78T= | |
NM_002256.3:c.*78T= | NP_002247.3:n.*78T= | |
XM_011509525.1:c.*78T= | XP_011507827.1:n.*78T= | |
NM_002256.4:c.*78T= MANE Select | NP_002247.3:n.*78T= |