HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225786C= , CM000668.2:g.3225786C= | GRCh38 |
NC_000006.11:g.3226020C= , CM000668.1:g.3226020C= | GRCh37 |
NC_000006.10:g.3171019C= | NCBI36 |
NG_016715.1:g.6949G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.303G= MANE Select | ENSP00000259818.6:p.Trp101= | |
ENST00000680070.1:n.1233G= | ||
ENST00000681707.1:n.1130G= | ||
ENST00000681757.1:n.608G= | ||
ENST00000259818.7:c.303G= | ENSP00000259818.6:p.Trp101= | |
ENST00000473006.1:n.420G= | ||
NM_178012.4:c.303G= | NP_821080.1:p.Trp101= | |
XM_011514571.1:c.87G= | XP_011512873.1:p.Trp29= | |
NM_178012.5:c.303G= MANE Select | NP_821080.1:p.Trp101= |