Canonical Allele Identifier: CA2123451464

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431432G= , CM000676.2:g.23431432G=	GRCh38
NC_000014.8:g.23900641G= , CM000676.1:g.23900641G=	GRCh37
NC_000014.7:g.22970481G=	NCBI36
NG_007884.1:g.9230C= , LRG_384:g.9230C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.782C= MANE Select	ENSP00000347507.3:p.Ala261=
ENST00000355349.3:c.782C=	ENSP00000347507.3:p.Ala261=
NM_000257.3:c.782C=	NP_000248.2:p.Ala261=
XR_245686.3:n.888C=
XM_017021340.1:c.782C=	XP_016876829.1:p.Ala261=
NM_000257.4:c.782C= MANE Select	NP_000248.2:p.Ala261=