Canonical Allele Identifier: CA1207023149
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652181T= , CM000663.2:g.171652181T= GRCh38
NC_000001.10:g.171621321T= , CM000663.1:g.171621321T= GRCh37
NC_000001.9:g.169887944T= NCBI36
NG_008859.1:g.5453A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.431A= MANE Select ENSP00000037502.5:p.Asn144=
ENST00000638471.1:c.130+301A= ENSP00000491206.1:n.130+301A=
ENST00000037502.10:c.431A= ENSP00000037502.5:p.Asn144=
ENST00000614688.1:c.431A= ENSP00000478680.1:p.Asn144=
NM_000261.1:c.431A= NP_000252.1:p.Asn144=
NM_000261.2:c.431A= MANE Select NP_000252.1:p.Asn144=