HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171636298A= , CM000663.2:g.171636298A= | GRCh38 |
NC_000001.10:g.171605438A= , CM000663.1:g.171605438A= | GRCh37 |
NC_000001.9:g.169872061A= | NCBI36 |
NG_008859.1:g.21336T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.1142T= (MYOC) MANE Select | ENSP00000037502.5:p.Leu381= | |
ENST00000637303.1:c.235-2332A= (MYOCOS) | ENSP00000490048.1:n.235-2332A= | |
ENST00000638471.1:c.*480T= (MYOC) | ENSP00000491206.1:n.*480T= | |
ENST00000037502.10:c.1142T= (MYOC) | ENSP00000037502.5:p.Leu381= | |
ENST00000614688.1:c.*106T= (MYOC) | ENSP00000478680.1:n.*106T= | |
NM_000261.1:c.1142T= (MYOC) | NP_000252.1:p.Leu381= | |
NM_000261.2:c.1142T= (MYOC) MANE Select | NP_000252.1:p.Leu381= |