Canonical Allele Identifier: CA891106044
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI

Linked Data

dbSNP Id: rs1397512664
gnomAD v3: 1-171635701-C-T
gnomAD v4: 1-171635701-C-T
MyVariant Identifiers: chr1:g.171604841C>T (hg19) chr1:g.171635701C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635701C>T , CM000663.2:g.171635701C>T GRCh38
NC_000001.10:g.171604841C>T , CM000663.1:g.171604841C>T GRCh37
NC_000001.9:g.169871464C>T NCBI36
NG_008859.1:g.21933G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*224G>A (MYOC) MANE Select ENSP00000037502.5:n.*224G>A
ENST00000637303.1:c.235-2929C>T (MYOCOS) ENSP00000490048.1:n.235-2929C>T
ENST00000638471.1:c.*1077G>A (MYOC) ENSP00000491206.1:n.*1077G>A
ENST00000037502.10:c.*224G>A (MYOC) ENSP00000037502.5:n.*224G>A
ENST00000614688.1:c.*703G>A (MYOC) ENSP00000478680.1:n.*703G>A
NM_000261.1:c.*224G>A (MYOC) NP_000252.1:n.*224G>A
NM_000261.2:c.*224G>A (MYOC) MANE Select NP_000252.1:n.*224G>A
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