HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586487G= , CM000673.2:g.67586487G= | GRCh38 |
NC_000011.9:g.67353958G= , CM000673.1:g.67353958G= | GRCh37 |
NC_000011.8:g.67110534G= | NCBI36 |
NG_012075.1:g.7893G= , LRG_723:g.7893G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.435G= | ENSP00000381604.1:p.Val145= | |
ENST00000398606.10:c.543G= MANE Select | ENSP00000381607.3:p.Val181= | |
ENST00000646888.1:c.*259G= | ENSP00000494477.1:n.*259G= | |
ENST00000398603.5:c.435G= | ENSP00000381604.1:p.Val145= | |
ENST00000398606.7:c.543G= | ENSP00000381607.3:p.Val181= | |
ENST00000467591.1:n.654G= | ||
ENST00000494593.1:n.1515G= | ||
ENST00000498765.5:c.606G= | ||
NM_000852.3:c.543G= , LRG_723t1:c.543G= | NP_000843.1:p.Val181= | |
NM_000852.4:c.543G= MANE Select | NP_000843.1:p.Val181= |