Canonical Allele Identifier: CA2123455930

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433653T= , CM000676.2:g.23433653T=	GRCh38
NC_000014.8:g.23902862T= , CM000676.1:g.23902862T=	GRCh37
NC_000014.7:g.22972702T=	NCBI36
NG_007884.1:g.7009A= , LRG_384:g.7009A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.80A= MANE Select	ENSP00000347507.3:p.Gln27=
ENST00000355349.3:c.80A=	ENSP00000347507.3:p.Gln27=
NM_000257.3:c.80A=	NP_000248.2:p.Gln27=
XR_245686.3:n.186A=
XM_017021340.1:c.80A=	XP_016876829.1:p.Gln27=
NM_000257.4:c.80A= MANE Select	NP_000248.2:p.Gln27=