Canonical Allele Identifier: CA2839481256
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635886C>T , CM000663.2:g.171635886C>T GRCh38
NC_000001.10:g.171605026C>T , CM000663.1:g.171605026C>T GRCh37
NC_000001.9:g.169871649C>T NCBI36
NG_008859.1:g.21748G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*39G>A (MYOC) MANE Select ENSP00000037502.5:n.*39G>A
ENST00000637303.1:c.235-2744C>T (MYOCOS) ENSP00000490048.1:n.235-2744C>T
ENST00000638471.1:c.*892G>A (MYOC) ENSP00000491206.1:n.*892G>A
ENST00000037502.10:c.*39G>A (MYOC) ENSP00000037502.5:n.*39G>A
ENST00000614688.1:c.*518G>A (MYOC) ENSP00000478680.1:n.*518G>A
NM_000261.1:c.*39G>A (MYOC) NP_000252.1:n.*39G>A
NM_000261.2:c.*39G>A (MYOC) MANE Select NP_000252.1:n.*39G>A
Search 100 bp 5'
Search 100 bp 3'