HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586540A>C , CM000673.2:g.67586540A>C | GRCh38 |
NC_000011.9:g.67354011A>C , CM000673.1:g.67354011A>C | GRCh37 |
NC_000011.8:g.67110587A>C | NCBI36 |
NG_012075.1:g.7946A>C , LRG_723:g.7946A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.488A>C | ENSP00000381604.1:p.Tyr163Ser | |
ENST00000398606.10:c.596A>C MANE Select | ENSP00000381607.3:p.Tyr199Ser | |
ENST00000398603.5:c.488A>C | ENSP00000381604.1:p.Tyr163Ser | |
ENST00000398606.7:c.596A>C | ENSP00000381607.3:p.Tyr199Ser | |
ENST00000467591.1:n.707A>C | ||
ENST00000494593.1:n.1568A>C | ||
ENST00000498765.5:c.659A>C | ||
NM_000852.3:c.596A>C , LRG_723t1:c.596A>C | NP_000843.1:p.Tyr199Ser | |
NM_000852.4:c.596A>C MANE Select | NP_000843.1:p.Tyr199Ser |