Canonical Allele Identifier: CA2123450611

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23430993A= , CM000676.2:g.23430993A=	GRCh38
NC_000014.8:g.23900202A= , CM000676.1:g.23900202A=	GRCh37
NC_000014.7:g.22970042A=	NCBI36
NG_007884.1:g.9669T= , LRG_384:g.9669T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.803T= MANE Select	ENSP00000347507.3:p.Leu268=
ENST00000355349.3:c.803T=	ENSP00000347507.3:p.Leu268=
NM_000257.3:c.803T=	NP_000248.2:p.Leu268=
XR_245686.3:n.909T=
XM_017021340.1:c.803T=	XP_016876829.1:p.Leu268=
NM_000257.4:c.803T= MANE Select	NP_000248.2:p.Leu268=