Canonical Allele Identifier: CA2123456488

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433998G= , CM000676.2:g.23433998G=	GRCh38
NC_000014.8:g.23903207G= , CM000676.1:g.23903207G=	GRCh37
NC_000014.7:g.22973047G=	NCBI36
NG_007884.1:g.6664C= , LRG_384:g.6664C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.-9+196C= MANE Select	ENSP00000347507.3:n.-9+196C=
ENST00000355349.3:c.-9+196C=	ENSP00000347507.3:n.-9+196C=
NM_000257.3:c.-9+196C=	NP_000248.2:n.-9+196C=
XR_245686.3:n.98+196C=
XM_017021340.1:c.-8-258C=	XP_016876829.1:n.-8-258C=
NM_000257.4:c.-9+196C= MANE Select	NP_000248.2:n.-9+196C=