Canonical Allele Identifier: CA2123450672

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431009G= , CM000676.2:g.23431009G=	GRCh38
NC_000014.8:g.23900218G= , CM000676.1:g.23900218G=	GRCh37
NC_000014.7:g.22970058G=	NCBI36
NG_007884.1:g.9653C= , LRG_384:g.9653C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.797-10C= MANE Select	ENSP00000347507.3:n.797-10C=
ENST00000355349.3:c.797-10C=	ENSP00000347507.3:n.797-10C=
NM_000257.3:c.797-10C=	NP_000248.2:n.797-10C=
XR_245686.3:n.903-10C=
XM_017021340.1:c.797-10C=	XP_016876829.1:n.797-10C=
NM_000257.4:c.797-10C= MANE Select	NP_000248.2:n.797-10C=