Canonical Allele Identifier: CA2123450554

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23430975A= , CM000676.2:g.23430975A=	GRCh38
NC_000014.8:g.23900184A= , CM000676.1:g.23900184A=	GRCh37
NC_000014.7:g.22970024A=	NCBI36
NG_007884.1:g.9687T= , LRG_384:g.9687T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.821T= MANE Select	ENSP00000347507.3:p.Ile274=
ENST00000355349.3:c.821T=	ENSP00000347507.3:p.Ile274=
NM_000257.3:c.821T=	NP_000248.2:p.Ile274=
XR_245686.3:n.927T=
XM_017021340.1:c.821T=	XP_016876829.1:p.Ile274=
NM_000257.4:c.821T= MANE Select	NP_000248.2:p.Ile274=