Canonical Allele Identifier: CA2123456579

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23434073T= , CM000676.2:g.23434073T=	GRCh38
NC_000014.8:g.23903282T= , CM000676.1:g.23903282T=	GRCh37
NC_000014.7:g.22973122T=	NCBI36
NG_007884.1:g.6589A= , LRG_384:g.6589A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.-9+121A= MANE Select	ENSP00000347507.3:n.-9+121A=
ENST00000355349.3:c.-9+121A=	ENSP00000347507.3:n.-9+121A=
NM_000257.3:c.-9+121A=	NP_000248.2:n.-9+121A=
XR_245686.3:n.98+121A=
XM_017021340.1:c.-8-333A=	XP_016876829.1:n.-8-333A=
NM_000257.4:c.-9+121A= MANE Select	NP_000248.2:n.-9+121A=