HGVS | Genome Assembly |
---|---|
NC_000002.12:g.84425579A= , CM000664.2:g.84425579A= | GRCh38 |
NC_000002.11:g.84652703A= , CM000664.1:g.84652703A= | GRCh37 |
NC_000002.10:g.84506214A= | NCBI36 |
NG_016755.1:g.38884T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393868.7:c.850T= MANE Select | ENSP00000377446.2:p.Ser284= | |
ENST00000651342.1:c.*290T= | ENSP00000498471.1:n.*290T= | |
ENST00000393868.6:c.850T= | ENSP00000377446.2:p.Ser284= | |
ENST00000484365.1:n.1358T= | ||
ENST00000487809.1:n.597T= | ||
ENST00000491123.5:n.696T= | ||
NM_003849.3:c.850T= | NP_003840.2:p.Ser284= | |
NM_003849.4:c.850T= MANE Select | NP_003840.2:p.Ser284= |