Canonical Allele Identifier: CA1141292089
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635859C= , CM000663.2:g.171635859C= GRCh38
NC_000001.10:g.171604999C= , CM000663.1:g.171604999C= GRCh37
NC_000001.9:g.169871622C= NCBI36
NG_008859.1:g.21775G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*66G= (MYOC) MANE Select ENSP00000037502.5:n.*66G=
ENST00000637303.1:c.235-2771C= (MYOCOS) ENSP00000490048.1:n.235-2771C=
ENST00000638471.1:c.*919G= (MYOC) ENSP00000491206.1:n.*919G=
ENST00000037502.10:c.*66G= (MYOC) ENSP00000037502.5:n.*66G=
ENST00000614688.1:c.*545G= (MYOC) ENSP00000478680.1:n.*545G=
NM_000261.1:c.*66G= (MYOC) NP_000252.1:n.*66G=
NM_000261.2:c.*66G= (MYOC) MANE Select NP_000252.1:n.*66G=
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