Canonical Allele Identifier: CA2123455823

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433593A= , CM000676.2:g.23433593A=	GRCh38
NC_000014.8:g.23902802A= , CM000676.1:g.23902802A=	GRCh37
NC_000014.7:g.22972642A=	NCBI36
NG_007884.1:g.7069T= , LRG_384:g.7069T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.140T= MANE Select	ENSP00000347507.3:p.Val47=
ENST00000355349.3:c.140T=	ENSP00000347507.3:p.Val47=
NM_000257.3:c.140T=	NP_000248.2:p.Val47=
XR_245686.3:n.246T=
XM_017021340.1:c.140T=	XP_016876829.1:p.Val47=
NM_000257.4:c.140T= MANE Select	NP_000248.2:p.Val47=