HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47377058A>C , CM000664.2:g.47377058A>C | GRCh38 |
NC_000002.11:g.47604197A>C , CM000664.1:g.47604197A>C | GRCh37 |
NC_000002.10:g.47457701A>C | NCBI36 |
NG_012352.2:g.36896A>C , LRG_215:g.36896A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263735.9:c.536A>C MANE Select | ENSP00000263735.4:p.Lys179Thr | |
ENST00000263735.8:c.536A>C | ENSP00000263735.4:p.Lys179Thr | |
ENST00000405271.5:c.620A>C | ENSP00000385476.1:p.Lys207Thr | |
ENST00000456133.5:c.620A>C | ENSP00000410675.1:p.Lys207Thr | |
ENST00000490733.1:n.385A>C | ||
NM_002354.2:c.536A>C , LRG_215t1:c.536A>C | NP_002345.2:p.Lys179Thr | |
NM_002354.3:c.536A>C MANE Select | NP_002345.2:p.Lys179Thr |