HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171636640T= , CM000663.2:g.171636640T= | GRCh38 |
NC_000001.10:g.171605780T= , CM000663.1:g.171605780T= | GRCh37 |
NC_000001.9:g.169872403T= | NCBI36 |
NG_008859.1:g.20994A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.800A= (MYOC) MANE Select | ENSP00000037502.5:p.Tyr267= | |
ENST00000637303.1:c.235-1990T= (MYOCOS) | ENSP00000490048.1:n.235-1990T= | |
ENST00000638471.1:c.*138A= (MYOC) | ENSP00000491206.1:n.*138A= | |
ENST00000037502.10:c.800A= (MYOC) | ENSP00000037502.5:p.Tyr267= | |
ENST00000614688.1:c.800A= (MYOC) | ENSP00000478680.1:p.Tyr267= | |
NM_000261.1:c.800A= (MYOC) | NP_000252.1:p.Tyr267= | |
NM_000261.2:c.800A= (MYOC) MANE Select | NP_000252.1:p.Tyr267= |