Canonical Allele Identifier: CA527265961
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI

Linked Data

dbSNP Id: rs1281277487
gnomAD v2: 1-171605884-T-C
gnomAD v3: 1-171636744-T-C
gnomAD v4: 1-171636744-T-C
MyVariant Identifiers: chr1:g.171605884T>C (hg19) chr1:g.171636744T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636744T>C , CM000663.2:g.171636744T>C GRCh38
NC_000001.10:g.171605884T>C , CM000663.1:g.171605884T>C GRCh37
NC_000001.9:g.169872507T>C NCBI36
NG_008859.1:g.20890A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.731-35A>G (MYOC) MANE Select ENSP00000037502.5:n.731-35A>G
ENST00000637303.1:c.235-1886T>C (MYOCOS) ENSP00000490048.1:n.235-1886T>C
ENST00000638471.1:c.*69-35A>G (MYOC) ENSP00000491206.1:n.*69-35A>G
ENST00000037502.10:c.731-35A>G (MYOC) ENSP00000037502.5:n.731-35A>G
ENST00000614688.1:c.731-35A>G (MYOC) ENSP00000478680.1:n.731-35A>G
NM_000261.1:c.731-35A>G (MYOC) NP_000252.1:n.731-35A>G
NM_000261.2:c.731-35A>G (MYOC) MANE Select NP_000252.1:n.731-35A>G
Search 100 bp 5'
Search 100 bp 3'