Canonical Allele Identifier: CA2123451436

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431426A= , CM000676.2:g.23431426A=	GRCh38
NC_000014.8:g.23900635A= , CM000676.1:g.23900635A=	GRCh37
NC_000014.7:g.22970475A=	NCBI36
NG_007884.1:g.9236T= , LRG_384:g.9236T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.788T= MANE Select	ENSP00000347507.3:p.Ile263=
ENST00000355349.3:c.788T=	ENSP00000347507.3:p.Ile263=
NM_000257.3:c.788T=	NP_000248.2:p.Ile263=
XR_245686.3:n.894T=
XM_017021340.1:c.788T=	XP_016876829.1:p.Ile263=
NM_000257.4:c.788T= MANE Select	NP_000248.2:p.Ile263=