Canonical Allele Identifier: CA421939411
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 2442270
ClinVar RCV Id: RCV003148599
MyVariant Identifiers: chr1:g.171621329G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652189G>A , CM000663.2:g.171652189G>A GRCh38
NC_000001.10:g.171621329G>A , CM000663.1:g.171621329G>A GRCh37
NC_000001.9:g.169887952G>A NCBI36
NG_008859.1:g.5445C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.423C>T MANE Select ENSP00000037502.5:p.Ala141=
ENST00000638471.1:c.130+293C>T ENSP00000491206.1:n.130+293C>T
ENST00000037502.10:c.423C>T ENSP00000037502.5:p.Ala141=
ENST00000614688.1:c.423C>T ENSP00000478680.1:p.Ala141=
NM_000261.1:c.423C>T NP_000252.1:p.Ala141=
NM_000261.2:c.423C>T MANE Select NP_000252.1:p.Ala141=