HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171636086C= , CM000663.2:g.171636086C= | GRCh38 |
NC_000001.10:g.171605226C= , CM000663.1:g.171605226C= | GRCh37 |
NC_000001.9:g.169871849C= | NCBI36 |
NG_008859.1:g.21548G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.1354G= (MYOC) MANE Select | ENSP00000037502.5:p.Ala452= | |
ENST00000637303.1:c.235-2544C= (MYOCOS) | ENSP00000490048.1:n.235-2544C= | |
ENST00000638471.1:c.*692G= (MYOC) | ENSP00000491206.1:n.*692G= | |
ENST00000037502.10:c.1354G= (MYOC) | ENSP00000037502.5:p.Ala452= | |
ENST00000614688.1:c.*318G= (MYOC) | ENSP00000478680.1:n.*318G= | |
NM_000261.1:c.1354G= (MYOC) | NP_000252.1:p.Ala452= | |
NM_000261.2:c.1354G= (MYOC) MANE Select | NP_000252.1:p.Ala452= |