Canonical Allele Identifier: CA1207023026
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171651828G= , CM000663.2:g.171651828G= GRCh38
NC_000001.10:g.171620968G= , CM000663.1:g.171620968G= GRCh37
NC_000001.9:g.169887591G= NCBI36
NG_008859.1:g.5806C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.604+180C= MANE Select ENSP00000037502.5:n.604+180C=
ENST00000638471.1:c.130+654C= ENSP00000491206.1:n.130+654C=
ENST00000037502.10:c.604+180C= ENSP00000037502.5:n.604+180C=
ENST00000614688.1:c.604+180C= ENSP00000478680.1:n.604+180C=
NM_000261.1:c.604+180C= NP_000252.1:n.604+180C=
NM_000261.2:c.604+180C= MANE Select NP_000252.1:n.604+180C=