Canonical Allele Identifier: CA2123450441

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23430939A= , CM000676.2:g.23430939A=	GRCh38
NC_000014.8:g.23900148A= , CM000676.1:g.23900148A=	GRCh37
NC_000014.7:g.22969988A=	NCBI36
NG_007884.1:g.9723T= , LRG_384:g.9723T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.857T= MANE Select	ENSP00000347507.3:p.Phe286=
ENST00000355349.3:c.857T=	ENSP00000347507.3:p.Phe286=
NM_000257.3:c.857T=	NP_000248.2:p.Phe286=
XR_245686.3:n.963T=
XM_017021340.1:c.857T=	XP_016876829.1:p.Phe286=
NM_000257.4:c.857T= MANE Select	NP_000248.2:p.Phe286=