HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586540A>G , CM000673.2:g.67586540A>G | GRCh38 |
NC_000011.9:g.67354011A>G , CM000673.1:g.67354011A>G | GRCh37 |
NC_000011.8:g.67110587A>G | NCBI36 |
NG_012075.1:g.7946A>G , LRG_723:g.7946A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.488A>G | ENSP00000381604.1:p.Tyr163Cys | |
ENST00000398606.10:c.596A>G MANE Select | ENSP00000381607.3:p.Tyr199Cys | |
ENST00000398603.5:c.488A>G | ENSP00000381604.1:p.Tyr163Cys | |
ENST00000398606.7:c.596A>G | ENSP00000381607.3:p.Tyr199Cys | |
ENST00000467591.1:n.707A>G | ||
ENST00000494593.1:n.1568A>G | ||
ENST00000498765.5:c.659A>G | ||
NM_000852.3:c.596A>G , LRG_723t1:c.596A>G | NP_000843.1:p.Tyr199Cys | |
NM_000852.4:c.596A>G MANE Select | NP_000843.1:p.Tyr199Cys |