HGVS | Genome Assembly |
---|---|
NC_000001.11:g.193251481T= , CM000663.2:g.193251481T= | GRCh38 |
NC_000001.10:g.193220611T= , CM000663.1:g.193220611T= | GRCh37 |
NC_000001.9:g.191487234T= | NCBI36 |
NG_012691.1:g.134524T= , LRG_507:g.134524T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367435.5:c.*769T= MANE Select | ENSP00000356405.4:n.*769T= | |
ENST00000635846.1:c.*769T= | ENSP00000490035.1:n.*769T= | |
ENST00000643006.1:c.*1275T= | ENSP00000496633.1:n.*1275T= | |
ENST00000367435.3:c.*769T= | ENSP00000356405.3:n.*769T= | |
NM_024529.4:c.*769T= , LRG_507t1:c.*769T= | NP_078805.3:n.*769T= | |
NM_024529.5:c.*769T= MANE Select | NP_078805.3:n.*769T= |