HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225585G= , CM000668.2:g.3225585G= | GRCh38 |
NC_000006.11:g.3225819G= , CM000668.1:g.3225819G= | GRCh37 |
NC_000006.10:g.3170818G= | NCBI36 |
NG_016715.1:g.7150C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.504C= MANE Select | ENSP00000259818.6:p.Ser168= | |
ENST00000680070.1:n.1434C= | ||
ENST00000681707.1:n.1331C= | ||
ENST00000681757.1:n.809C= | ||
ENST00000259818.7:c.504C= | ENSP00000259818.6:p.Ser168= | |
ENST00000473006.1:n.621C= | ||
NM_178012.4:c.504C= | NP_821080.1:p.Ser168= | |
XM_011514571.1:c.288C= | XP_011512873.1:p.Ser96= | |
NM_178012.5:c.504C= MANE Select | NP_821080.1:p.Ser168= |