Canonical Allele Identifier: CA1207016597
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635657A= , CM000663.2:g.171635657A= GRCh38
NC_000001.10:g.171604797A= , CM000663.1:g.171604797A= GRCh37
NC_000001.9:g.169871420A= NCBI36
NG_008859.1:g.21977T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*268T= (MYOC) MANE Select ENSP00000037502.5:n.*268T=
ENST00000637303.1:c.235-2973A= (MYOCOS) ENSP00000490048.1:n.235-2973A=
ENST00000638471.1:c.*1121T= (MYOC) ENSP00000491206.1:n.*1121T=
ENST00000037502.10:c.*268T= (MYOC) ENSP00000037502.5:n.*268T=
ENST00000614688.1:c.*747T= (MYOC) ENSP00000478680.1:n.*747T=
NM_000261.1:c.*268T= (MYOC) NP_000252.1:n.*268T=
NM_000261.2:c.*268T= (MYOC) MANE Select NP_000252.1:n.*268T=
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