Canonical Allele Identifier: CA1144389012

Gene: MYOC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171651822T= , CM000663.2:g.171651822T=	GRCh38
NC_000001.10:g.171620962T= , CM000663.1:g.171620962T=	GRCh37
NC_000001.9:g.169887585T=	NCBI36
NG_008859.1:g.5812A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000037502.11:c.604+186A= MANE Select	ENSP00000037502.5:n.604+186A=
ENST00000638471.1:c.130+660A=	ENSP00000491206.1:n.130+660A=
ENST00000037502.10:c.604+186A=	ENSP00000037502.5:n.604+186A=
ENST00000614688.1:c.604+186A=	ENSP00000478680.1:n.604+186A=
NM_000261.1:c.604+186A=	NP_000252.1:n.604+186A=
NM_000261.2:c.604+186A= MANE Select	NP_000252.1:n.604+186A=