Canonical Allele Identifier: CA2123455851

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23424826C= , CM000676.2:g.23424826C=	GRCh38
NC_000014.8:g.23894035C= , CM000676.1:g.23894035C=	GRCh37
NC_000014.7:g.22963875C=	NCBI36
NG_007884.1:g.15836G= , LRG_384:g.15836G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.2622G= MANE Select	ENSP00000347507.3:p.Glu874=
ENST00000355349.3:c.2622G=	ENSP00000347507.3:p.Glu874=
NM_000257.3:c.2622G=	NP_000248.2:p.Glu874=
XR_245686.3:n.2728G=
XM_017021340.1:c.2622G=	XP_016876829.1:p.Glu874=
NM_000257.4:c.2622G= MANE Select	NP_000248.2:p.Glu874=