Canonical Allele Identifier: CA1207023293
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652643G= , CM000663.2:g.171652643G= GRCh38
NC_000001.10:g.171621783G= , CM000663.1:g.171621783G= GRCh37
NC_000001.9:g.169888406G= NCBI36
NG_008859.1:g.4991C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.-32C= MANE Select ENSP00000037502.5:n.-32C=
ENST00000037502.10:c.-32C= ENSP00000037502.5:n.-32C=
NM_000261.2:c.-32C= MANE Select NP_000252.1:n.-32C=