Canonical Allele Identifier: CA2123461766

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23415056T= , CM000676.2:g.23415056T=	GRCh38
NC_000014.8:g.23884265T= , CM000676.1:g.23884265T=	GRCh37
NC_000014.7:g.22954105T=	NCBI36
NG_007884.1:g.25606A= , LRG_384:g.25606A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.5498A= MANE Select	ENSP00000347507.3:p.Asn1833=
ENST00000355349.3:c.5498A=	ENSP00000347507.3:p.Asn1833=
NM_000257.3:c.5498A=	NP_000248.2:p.Asn1833=
XM_017021340.1:c.5498A=	XP_016876829.1:p.Asn1833=
NM_000257.4:c.5498A= MANE Select	NP_000248.2:p.Asn1833=