Canonical Allele Identifier: CA2123456014

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433683C= , CM000676.2:g.23433683C=	GRCh38
NC_000014.8:g.23902892C= , CM000676.1:g.23902892C=	GRCh37
NC_000014.7:g.22972732C=	NCBI36
NG_007884.1:g.6979G= , LRG_384:g.6979G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.50G= MANE Select	ENSP00000347507.3:p.Arg17=
ENST00000355349.3:c.50G=	ENSP00000347507.3:p.Arg17=
NM_000257.3:c.50G=	NP_000248.2:p.Arg17=
XR_245686.3:n.156G=
XM_017021340.1:c.50G=	XP_016876829.1:p.Arg17=
NM_000257.4:c.50G= MANE Select	NP_000248.2:p.Arg17=