HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171635603C>A , CM000663.2:g.171635603C>A | GRCh38 |
NC_000001.10:g.171604743C>A , CM000663.1:g.171604743C>A | GRCh37 |
NC_000001.9:g.169871366C>A | NCBI36 |
NG_008859.1:g.22031G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.*322G>T (MYOC) MANE Select | ENSP00000037502.5:n.*322G>T | |
ENST00000637303.1:c.235-3027C>A (MYOCOS) | ENSP00000490048.1:n.235-3027C>A | |
ENST00000638471.1:c.*1175G>T (MYOC) | ENSP00000491206.1:n.*1175G>T | |
ENST00000037502.10:c.*322G>T (MYOC) | ENSP00000037502.5:n.*322G>T | |
ENST00000614688.1:c.*801G>T (MYOC) | ENSP00000478680.1:n.*801G>T | |
NM_000261.1:c.*322G>T (MYOC) | NP_000252.1:n.*322G>T | |
NM_000261.2:c.*322G>T (MYOC) MANE Select | NP_000252.1:n.*322G>T |