HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171635735T= , CM000663.2:g.171635735T= | GRCh38 |
NC_000001.10:g.171604875T= , CM000663.1:g.171604875T= | GRCh37 |
NC_000001.9:g.169871498T= | NCBI36 |
NG_008859.1:g.21899A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.*190A= (MYOC) MANE Select | ENSP00000037502.5:n.*190A= | |
ENST00000637303.1:c.235-2895T= (MYOCOS) | ENSP00000490048.1:n.235-2895T= | |
ENST00000638471.1:c.*1043A= (MYOC) | ENSP00000491206.1:n.*1043A= | |
ENST00000037502.10:c.*190A= (MYOC) | ENSP00000037502.5:n.*190A= | |
ENST00000614688.1:c.*669A= (MYOC) | ENSP00000478680.1:n.*669A= | |
NM_000261.1:c.*190A= (MYOC) | NP_000252.1:n.*190A= | |
NM_000261.2:c.*190A= (MYOC) MANE Select | NP_000252.1:n.*190A= |