HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586488G= , CM000673.2:g.67586488G= | GRCh38 |
NC_000011.9:g.67353959G= , CM000673.1:g.67353959G= | GRCh37 |
NC_000011.8:g.67110535G= | NCBI36 |
NG_012075.1:g.7894G= , LRG_723:g.7894G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.436G= | ENSP00000381604.1:p.Gly146= | |
ENST00000398606.10:c.544G= MANE Select | ENSP00000381607.3:p.Gly182= | |
ENST00000646888.1:c.*260G= | ENSP00000494477.1:n.*260G= | |
ENST00000398603.5:c.436G= | ENSP00000381604.1:p.Gly146= | |
ENST00000398606.7:c.544G= | ENSP00000381607.3:p.Gly182= | |
ENST00000467591.1:n.655G= | ||
ENST00000494593.1:n.1516G= | ||
ENST00000498765.5:c.607G= | ||
NM_000852.3:c.544G= , LRG_723t1:c.544G= | NP_000843.1:p.Gly182= | |
NM_000852.4:c.544G= MANE Select | NP_000843.1:p.Gly182= |