Canonical Allele Identifier: CA2123456010

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433681T= , CM000676.2:g.23433681T=	GRCh38
NC_000014.8:g.23902890T= , CM000676.1:g.23902890T=	GRCh37
NC_000014.7:g.22972730T=	NCBI36
NG_007884.1:g.6981A= , LRG_384:g.6981A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.52A= MANE Select	ENSP00000347507.3:p.Lys18=
ENST00000355349.3:c.52A=	ENSP00000347507.3:p.Lys18=
NM_000257.3:c.52A=	NP_000248.2:p.Lys18=
XR_245686.3:n.158A=
XM_017021340.1:c.52A=	XP_016876829.1:p.Lys18=
NM_000257.4:c.52A= MANE Select	NP_000248.2:p.Lys18=