HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151871C>G , CM000681.2:g.55151871C>G | GRCh38 |
NC_000019.9:g.55663239C>G , CM000681.1:g.55663239C>G | GRCh37 |
NC_000019.8:g.60355051C>G | NCBI36 |
NG_007866.2:g.10862G>C , LRG_432:g.10862G>C | |
NG_011829.2:g.2368G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.596G>C MANE Select | ENSP00000341838.5:p.Ser199Thr | |
ENST00000665070.1:c.629G>C | ENSP00000499482.1:p.Ser210Thr | |
ENST00000344887.9:c.596G>C | ENSP00000341838.5:p.Ser199Thr | |
ENST00000585806.5:n.595G>C | ||
ENST00000588882.1:c.521G>C | ENSP00000466729.1:p.Ser174Thr | |
ENST00000589864.1:n.424G>C | ||
NM_000363.4:c.596G>C , LRG_432t1:c.596G>C | NP_000354.4:p.Ser199Thr | |
NM_000363.5:c.596G>C MANE Select | NP_000354.4:p.Ser199Thr |