Canonical Allele Identifier: CA421939409
Gene: MYOC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.171621326G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652186G>A , CM000663.2:g.171652186G>A GRCh38
NC_000001.10:g.171621326G>A , CM000663.1:g.171621326G>A GRCh37
NC_000001.9:g.169887949G>A NCBI36
NG_008859.1:g.5448C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.426C>T MANE Select ENSP00000037502.5:p.Tyr142=
ENST00000638471.1:c.130+296C>T ENSP00000491206.1:n.130+296C>T
ENST00000037502.10:c.426C>T ENSP00000037502.5:p.Tyr142=
ENST00000614688.1:c.426C>T ENSP00000478680.1:p.Tyr142=
NM_000261.1:c.426C>T NP_000252.1:p.Tyr142=
NM_000261.2:c.426C>T MANE Select NP_000252.1:p.Tyr142=