Canonical Allele Identifier: CA421938698
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.171605284G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636144G>T , CM000663.2:g.171636144G>T GRCh38
NC_000001.10:g.171605284G>T , CM000663.1:g.171605284G>T GRCh37
NC_000001.9:g.169871907G>T NCBI36
NG_008859.1:g.21490C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1296C>A (MYOC) MANE Select ENSP00000037502.5:p.Ile432=
ENST00000637303.1:c.235-2486G>T (MYOCOS) ENSP00000490048.1:n.235-2486G>T
ENST00000638471.1:c.*634C>A (MYOC) ENSP00000491206.1:n.*634C>A
ENST00000037502.10:c.1296C>A (MYOC) ENSP00000037502.5:p.Ile432=
ENST00000614688.1:c.*260C>A (MYOC) ENSP00000478680.1:n.*260C>A
NM_000261.1:c.1296C>A (MYOC) NP_000252.1:p.Ile432=
NM_000261.2:c.1296C>A (MYOC) MANE Select NP_000252.1:p.Ile432=
Search 100 bp 5'
Search 100 bp 3'