Canonical Allele Identifier: CA2123454691

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23424122C= , CM000676.2:g.23424122C=	GRCh38
NC_000014.8:g.23893331C= , CM000676.1:g.23893331C=	GRCh37
NC_000014.7:g.22963171C=	NCBI36
NG_007884.1:g.16540G= , LRG_384:g.16540G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.2707G= MANE Select	ENSP00000347507.3:p.Glu903=
ENST00000355349.3:c.2707G=	ENSP00000347507.3:p.Glu903=
NM_000257.3:c.2707G=	NP_000248.2:p.Glu903=
XR_245686.3:n.2813G=
XM_017021340.1:c.2707G=	XP_016876829.1:p.Glu903=
NM_000257.4:c.2707G= MANE Select	NP_000248.2:p.Glu903=