Canonical Allele Identifier: CA2123451209

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431357G= , CM000676.2:g.23431357G=	GRCh38
NC_000014.8:g.23900566G= , CM000676.1:g.23900566G=	GRCh37
NC_000014.7:g.22970406G=	NCBI36
NG_007884.1:g.9305C= , LRG_384:g.9305C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.796+61C= MANE Select	ENSP00000347507.3:n.796+61C=
ENST00000355349.3:c.796+61C=	ENSP00000347507.3:n.796+61C=
NM_000257.3:c.796+61C=	NP_000248.2:n.796+61C=
XR_245686.3:n.902+61C=
XM_017021340.1:c.796+61C=	XP_016876829.1:n.796+61C=
NM_000257.4:c.796+61C= MANE Select	NP_000248.2:n.796+61C=