HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32814370G= , CM000668.2:g.32814370G= | GRCh38 |
NC_000006.11:g.32782147G= , CM000668.1:g.32782147G= | GRCh37 |
NC_000006.10:g.32890125G= | NCBI36 |
NG_009793.3:g.29401C= | |
NG_012008.1:g.7679C= | |
NG_009793.4:g.29401C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000438763.7:c.593C= MANE Select | ENSP00000390020.2:p.Thr198= | |
ENST00000648009.1:c.593C= | ENSP00000496848.1:p.Thr198= | |
ENST00000438763.6:c.593C= | ENSP00000390020.2:p.Thr198= | |
ENST00000447394.1:c.543C= | ||
ENST00000452392.2:c.2414C= | ENSP00000391806.2:p.Thr805= | |
ENST00000475235.1:n.630C= | ||
ENST00000488325.5:c.*364C= | ENSP00000436618.1:n.*364C= | |
NM_002120.3:c.593C= | NP_002111.1:p.Thr198= | |
NM_002120.4:c.593C= MANE Select | NP_002111.1:p.Thr198= |