HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171636144G>A , CM000663.2:g.171636144G>A | GRCh38 |
NC_000001.10:g.171605284G>A , CM000663.1:g.171605284G>A | GRCh37 |
NC_000001.9:g.169871907G>A | NCBI36 |
NG_008859.1:g.21490C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000037502.11:c.1296C>T (MYOC) MANE Select | ENSP00000037502.5:p.Ile432= | |
ENST00000637303.1:c.235-2486G>A (MYOCOS) | ENSP00000490048.1:n.235-2486G>A | |
ENST00000638471.1:c.*634C>T (MYOC) | ENSP00000491206.1:n.*634C>T | |
ENST00000037502.10:c.1296C>T (MYOC) | ENSP00000037502.5:p.Ile432= | |
ENST00000614688.1:c.*260C>T (MYOC) | ENSP00000478680.1:n.*260C>T | |
NM_000261.1:c.1296C>T (MYOC) | NP_000252.1:p.Ile432= | |
NM_000261.2:c.1296C>T (MYOC) MANE Select | NP_000252.1:p.Ile432= |