HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171635955G>C , CM000663.2:g.171635955G>C | GRCh38 |
NC_000001.10:g.171605095G>C , CM000663.1:g.171605095G>C | GRCh37 |
NC_000001.9:g.169871718G>C | NCBI36 |
NG_008859.1:g.21679C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.1485C>G (MYOC) MANE Select | ENSP00000037502.5:p.Val495= | |
ENST00000637303.1:c.235-2675G>C (MYOCOS) | ENSP00000490048.1:n.235-2675G>C | |
ENST00000638471.1:c.*823C>G (MYOC) | ENSP00000491206.1:n.*823C>G | |
ENST00000037502.10:c.1485C>G (MYOC) | ENSP00000037502.5:p.Val495= | |
ENST00000614688.1:c.*449C>G (MYOC) | ENSP00000478680.1:n.*449C>G | |
NM_000261.1:c.1485C>G (MYOC) | NP_000252.1:p.Val495= | |
NM_000261.2:c.1485C>G (MYOC) MANE Select | NP_000252.1:p.Val495= |