HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586478A>G , CM000673.2:g.67586478A>G | GRCh38 |
NC_000011.9:g.67353949A>G , CM000673.1:g.67353949A>G | GRCh37 |
NC_000011.8:g.67110525A>G | NCBI36 |
NG_012075.1:g.7884A>G , LRG_723:g.7884A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.426A>G | ENSP00000381604.1:p.Ser142= | |
ENST00000398606.10:c.534A>G MANE Select | ENSP00000381607.3:p.Ser178= | |
ENST00000646888.1:c.*250A>G | ENSP00000494477.1:n.*250A>G | |
ENST00000398603.5:c.426A>G | ENSP00000381604.1:p.Ser142= | |
ENST00000398606.7:c.534A>G | ENSP00000381607.3:p.Ser178= | |
ENST00000467591.1:n.645A>G | ||
ENST00000494593.1:n.1506A>G | ||
ENST00000498765.5:c.597A>G | ||
NM_000852.3:c.534A>G , LRG_723t1:c.534A>G | NP_000843.1:p.Ser178= | |
NM_000852.4:c.534A>G MANE Select | NP_000843.1:p.Ser178= |