HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225593T= , CM000668.2:g.3225593T= | GRCh38 |
NC_000006.11:g.3225827T= , CM000668.1:g.3225827T= | GRCh37 |
NC_000006.10:g.3170826T= | NCBI36 |
NG_016715.1:g.7142A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.496A= MANE Select | ENSP00000259818.6:p.Thr166= | |
ENST00000680070.1:n.1426A= | ||
ENST00000681707.1:n.1323A= | ||
ENST00000681757.1:n.801A= | ||
ENST00000259818.7:c.496A= | ENSP00000259818.6:p.Thr166= | |
ENST00000473006.1:n.613A= | ||
NM_178012.4:c.496A= | NP_821080.1:p.Thr166= | |
XM_011514571.1:c.280A= | XP_011512873.1:p.Thr94= | |
NM_178012.5:c.496A= MANE Select | NP_821080.1:p.Thr166= |