Canonical Allele Identifier: CA421938639
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.171605206A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636066A>C , CM000663.2:g.171636066A>C GRCh38
NC_000001.10:g.171605206A>C , CM000663.1:g.171605206A>C GRCh37
NC_000001.9:g.169871829A>C NCBI36
NG_008859.1:g.21568T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1374T>G (MYOC) MANE Select ENSP00000037502.5:p.Gly458=
ENST00000637303.1:c.235-2564A>C (MYOCOS) ENSP00000490048.1:n.235-2564A>C
ENST00000638471.1:c.*712T>G (MYOC) ENSP00000491206.1:n.*712T>G
ENST00000037502.10:c.1374T>G (MYOC) ENSP00000037502.5:p.Gly458=
ENST00000614688.1:c.*338T>G (MYOC) ENSP00000478680.1:n.*338T>G
NM_000261.1:c.1374T>G (MYOC) NP_000252.1:p.Gly458=
NM_000261.2:c.1374T>G (MYOC) MANE Select NP_000252.1:p.Gly458=
Search 100 bp 5'
Search 100 bp 3'