HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171635873dup , CM000663.2:g.171635873dup | GRCh38 |
NC_000001.10:g.171605013dup , CM000663.1:g.171605013dup | GRCh37 |
NC_000001.9:g.169871636dup | NCBI36 |
NG_008859.1:g.21766dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.*57dup (MYOC) MANE Select | ENSP00000037502.5:n.*57dup | |
ENST00000637303.1:c.235-2757dup (MYOCOS) | ENSP00000490048.1:n.235-2757dup | |
ENST00000638471.1:c.*910dup (MYOC) | ENSP00000491206.1:n.*910dup | |
ENST00000037502.10:c.*57dup (MYOC) | ENSP00000037502.5:n.*57dup | |
ENST00000614688.1:c.*536dup (MYOC) | ENSP00000478680.1:n.*536dup | |
NM_000261.1:c.*57dup (MYOC) | NP_000252.1:n.*57dup | |
NM_000261.2:c.*57dup (MYOC) MANE Select | NP_000252.1:n.*57dup |