HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171636602del , CM000663.2:g.171636602del | GRCh38 |
NC_000001.10:g.171605742del , CM000663.1:g.171605742del | GRCh37 |
NC_000001.9:g.169872365del | NCBI36 |
NG_008859.1:g.21032del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.838del (MYOC) MANE Select | ENSP00000037502.5:p.Tyr280ThrfsTer? | |
ENST00000637303.1:c.235-2028del (MYOCOS) | ENSP00000490048.1:n.235-2028del | |
ENST00000638471.1:c.*176del (MYOC) | ENSP00000491206.1:n.*176del | |
ENST00000037502.10:c.838del (MYOC) | ENSP00000037502.5:p.Tyr280ThrfsTer? | |
ENST00000614688.1:c.838del (MYOC) | ENSP00000478680.1:p.Tyr280ThrfsTer? | |
NM_000261.1:c.838del (MYOC) | NP_000252.1:p.Tyr280ThrfsTer? | |
NM_000261.2:c.838del (MYOC) MANE Select | NP_000252.1:p.Tyr280ThrfsTer? |