HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171636337T= , CM000663.2:g.171636337T= | GRCh38 |
NC_000001.10:g.171605477T= , CM000663.1:g.171605477T= | GRCh37 |
NC_000001.9:g.169872100T= | NCBI36 |
NG_008859.1:g.21297A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.1103A= (MYOC) MANE Select | ENSP00000037502.5:p.Gln368= | |
ENST00000637303.1:c.235-2293T= (MYOCOS) | ENSP00000490048.1:n.235-2293T= | |
ENST00000638471.1:c.*441A= (MYOC) | ENSP00000491206.1:n.*441A= | |
ENST00000037502.10:c.1103A= (MYOC) | ENSP00000037502.5:p.Gln368= | |
ENST00000614688.1:c.*67A= (MYOC) | ENSP00000478680.1:n.*67A= | |
NM_000261.1:c.1103A= (MYOC) | NP_000252.1:p.Gln368= | |
NM_000261.2:c.1103A= (MYOC) MANE Select | NP_000252.1:p.Gln368= |