HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171635584G= , CM000663.2:g.171635584G= | GRCh38 |
NC_000001.10:g.171604724G= , CM000663.1:g.171604724G= | GRCh37 |
NC_000001.9:g.169871347G= | NCBI36 |
NG_008859.1:g.22050C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.*341C= (MYOC) MANE Select | ENSP00000037502.5:n.*341C= | |
ENST00000637303.1:c.235-3046G= (MYOCOS) | ENSP00000490048.1:n.235-3046G= | |
ENST00000638471.1:c.*1194C= (MYOC) | ENSP00000491206.1:n.*1194C= | |
ENST00000037502.10:c.*341C= (MYOC) | ENSP00000037502.5:n.*341C= | |
ENST00000614688.1:c.*820C= (MYOC) | ENSP00000478680.1:n.*820C= | |
NM_000261.1:c.*341C= (MYOC) | NP_000252.1:n.*341C= | |
NM_000261.2:c.*341C= (MYOC) MANE Select | NP_000252.1:n.*341C= |