Canonical Allele Identifier: CA10586137
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI

Linked Data

ClinVar Variation Id: 252960
ClinVar RCV Id: RCV000239401 RCV003319978
dbSNP Id: rs879255525
MyVariant Identifiers: chr1:g.171605757T>A (hg19) chr1:g.171636617T>A (hg38)
ERepo: CA10586137/MONDO:0007665/019
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636617T>A , CM000663.2:g.171636617T>A GRCh38
NC_000001.10:g.171605757T>A , CM000663.1:g.171605757T>A GRCh37
NC_000001.9:g.169872380T>A NCBI36
NG_008859.1:g.21017A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.823A>T (MYOC) MANE Select ENSP00000037502.5:p.Lys275Ter
ENST00000637303.1:c.235-2013T>A (MYOCOS) ENSP00000490048.1:n.235-2013T>A
ENST00000638471.1:c.*161A>T (MYOC) ENSP00000491206.1:n.*161A>T
ENST00000037502.10:c.823A>T (MYOC) ENSP00000037502.5:p.Lys275Ter
ENST00000614688.1:c.823A>T (MYOC) ENSP00000478680.1:p.Lys275Ter
NM_000261.1:c.823A>T (MYOC) NP_000252.1:p.Lys275Ter
NM_000261.2:c.823A>T (MYOC) MANE Select NP_000252.1:p.Lys275Ter
Search 100 bp 5'
Search 100 bp 3'