HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171636680G>T , CM000663.2:g.171636680G>T | GRCh38 |
NC_000001.10:g.171605820G>T , CM000663.1:g.171605820G>T | GRCh37 |
NC_000001.9:g.169872443G>T | NCBI36 |
NG_008859.1:g.20954C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.760C>A (MYOC) MANE Select | ENSP00000037502.5:p.Pro254Thr | |
ENST00000637303.1:c.235-1950G>T (MYOCOS) | ENSP00000490048.1:n.235-1950G>T | |
ENST00000638471.1:c.*98C>A (MYOC) | ENSP00000491206.1:n.*98C>A | |
ENST00000037502.10:c.760C>A (MYOC) | ENSP00000037502.5:p.Pro254Thr | |
ENST00000614688.1:c.760C>A (MYOC) | ENSP00000478680.1:p.Pro254Thr | |
NM_000261.1:c.760C>A (MYOC) | NP_000252.1:p.Pro254Thr | |
NM_000261.2:c.760C>A (MYOC) MANE Select | NP_000252.1:p.Pro254Thr |