Canonical Allele Identifier: CA1207016602
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI

Linked Data

dbSNP Id: rs1652900625
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635681C>T , CM000663.2:g.171635681C>T GRCh38
NC_000001.10:g.171604821C>T , CM000663.1:g.171604821C>T GRCh37
NC_000001.9:g.169871444C>T NCBI36
NG_008859.1:g.21953G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*244G>A (MYOC) MANE Select ENSP00000037502.5:n.*244G>A
ENST00000637303.1:c.235-2949C>T (MYOCOS) ENSP00000490048.1:n.235-2949C>T
ENST00000638471.1:c.*1097G>A (MYOC) ENSP00000491206.1:n.*1097G>A
ENST00000037502.10:c.*244G>A (MYOC) ENSP00000037502.5:n.*244G>A
ENST00000614688.1:c.*723G>A (MYOC) ENSP00000478680.1:n.*723G>A
NM_000261.1:c.*244G>A (MYOC) NP_000252.1:n.*244G>A
NM_000261.2:c.*244G>A (MYOC) MANE Select NP_000252.1:n.*244G>A
Search 100 bp 5'
Search 100 bp 3'