Canonical Allele Identifier: CA1207023055
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171651913G= , CM000663.2:g.171651913G= GRCh38
NC_000001.10:g.171621053G= , CM000663.1:g.171621053G= GRCh37
NC_000001.9:g.169887676G= NCBI36
NG_008859.1:g.5721C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.604+95C= MANE Select ENSP00000037502.5:n.604+95C=
ENST00000638471.1:c.130+569C= ENSP00000491206.1:n.130+569C=
ENST00000037502.10:c.604+95C= ENSP00000037502.5:n.604+95C=
ENST00000614688.1:c.604+95C= ENSP00000478680.1:n.604+95C=
NM_000261.1:c.604+95C= NP_000252.1:n.604+95C=
NM_000261.2:c.604+95C= MANE Select NP_000252.1:n.604+95C=