Canonical Allele Identifier: CA1207023232
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652402G= , CM000663.2:g.171652402G= GRCh38
NC_000001.10:g.171621542G= , CM000663.1:g.171621542G= GRCh37
NC_000001.9:g.169888165G= NCBI36
NG_008859.1:g.5232C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.210C= MANE Select ENSP00000037502.5:p.Val70=
ENST00000638471.1:c.130+80C= ENSP00000491206.1:n.130+80C=
ENST00000037502.10:c.210C= ENSP00000037502.5:p.Val70=
ENST00000614688.1:c.210C= ENSP00000478680.1:p.Val70=
NM_000261.1:c.210C= NP_000252.1:p.Val70=
NM_000261.2:c.210C= MANE Select NP_000252.1:p.Val70=