Canonical Allele Identifier: CA2123451531

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431450G= , CM000676.2:g.23431450G=	GRCh38
NC_000014.8:g.23900659G= , CM000676.1:g.23900659G=	GRCh37
NC_000014.7:g.22970499G=	NCBI36
NG_007884.1:g.9212C= , LRG_384:g.9212C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.764C= MANE Select	ENSP00000347507.3:p.Thr255=
ENST00000355349.3:c.764C=	ENSP00000347507.3:p.Thr255=
NM_000257.3:c.764C=	NP_000248.2:p.Thr255=
XR_245686.3:n.870C=
XM_017021340.1:c.764C=	XP_016876829.1:p.Thr255=
NM_000257.4:c.764C= MANE Select	NP_000248.2:p.Thr255=