Canonical Allele Identifier: CA2123455779

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433573G= , CM000676.2:g.23433573G=	GRCh38
NC_000014.8:g.23902782G= , CM000676.1:g.23902782G=	GRCh37
NC_000014.7:g.22972622G=	NCBI36
NG_007884.1:g.7089C= , LRG_384:g.7089C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.160C= MANE Select	ENSP00000347507.3:p.Arg54=
ENST00000355349.3:c.160C=	ENSP00000347507.3:p.Arg54=
NM_000257.3:c.160C=	NP_000248.2:p.Arg54=
XR_245686.3:n.266C=
XM_017021340.1:c.160C=	XP_016876829.1:p.Arg54=
NM_000257.4:c.160C= MANE Select	NP_000248.2:p.Arg54=