Canonical Allele Identifier: CA2123452149

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431621A= , CM000676.2:g.23431621A=	GRCh38
NC_000014.8:g.23900830A= , CM000676.1:g.23900830A=	GRCh37
NC_000014.7:g.22970670A=	NCBI36
NG_007884.1:g.9041T= , LRG_384:g.9041T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.696T= MANE Select	ENSP00000347507.3:p.Asn232=
ENST00000355349.3:c.696T=	ENSP00000347507.3:p.Asn232=
NM_000257.3:c.696T=	NP_000248.2:p.Asn232=
XR_245686.3:n.802T=
XM_017021340.1:c.696T=	XP_016876829.1:p.Asn232=
NM_000257.4:c.696T= MANE Select	NP_000248.2:p.Asn232=