Canonical Allele Identifier: CA1207023172
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652229C= , CM000663.2:g.171652229C= GRCh38
NC_000001.10:g.171621369C= , CM000663.1:g.171621369C= GRCh37
NC_000001.9:g.169887992C= NCBI36
NG_008859.1:g.5405G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.383G= MANE Select ENSP00000037502.5:p.Arg128=
ENST00000638471.1:c.130+253G= ENSP00000491206.1:n.130+253G=
ENST00000037502.10:c.383G= ENSP00000037502.5:p.Arg128=
ENST00000614688.1:c.383G= ENSP00000478680.1:p.Arg128=
NM_000261.1:c.383G= NP_000252.1:p.Arg128=
NM_000261.2:c.383G= MANE Select NP_000252.1:p.Arg128=