HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171638716G>A , CM000663.2:g.171638716G>A | GRCh38 |
NC_000001.10:g.171607856G>A , CM000663.1:g.171607856G>A | GRCh37 |
NC_000001.9:g.169874479G>A | NCBI36 |
NG_008859.1:g.18918C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.611C>T (MYOC) MANE Select | ENSP00000037502.5:p.Thr204Met | |
ENST00000637303.1:c.321G>A (MYOCOS) | ENSP00000490048.1:p.Thr107= | |
ENST00000638471.1:c.141C>T (MYOC) | ENSP00000491206.1:p.Tyr47= | |
ENST00000037502.10:c.611C>T (MYOC) | ENSP00000037502.5:p.Thr204Met | |
ENST00000614688.1:c.611C>T (MYOC) | ENSP00000478680.1:p.Thr204Met | |
NM_000261.1:c.611C>T (MYOC) | NP_000252.1:p.Thr204Met | |
NM_000261.2:c.611C>T (MYOC) MANE Select | NP_000252.1:p.Thr204Met |