Canonical Allele Identifier: CA1143452443
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652230G= , CM000663.2:g.171652230G= GRCh38
NC_000001.10:g.171621370G= , CM000663.1:g.171621370G= GRCh37
NC_000001.9:g.169887993G= NCBI36
NG_008859.1:g.5404C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.382C= MANE Select ENSP00000037502.5:p.Arg128=
ENST00000638471.1:c.130+252C= ENSP00000491206.1:n.130+252C=
ENST00000037502.10:c.382C= ENSP00000037502.5:p.Arg128=
ENST00000614688.1:c.382C= ENSP00000478680.1:p.Arg128=
NM_000261.1:c.382C= NP_000252.1:p.Arg128=
NM_000261.2:c.382C= MANE Select NP_000252.1:p.Arg128=