Canonical Allele Identifier: CA2123453988

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423947A= , CM000676.2:g.23423947A=	GRCh38
NC_000014.8:g.23893156A= , CM000676.1:g.23893156A=	GRCh37
NC_000014.7:g.22962996A=	NCBI36
NG_007884.1:g.16715T= , LRG_384:g.16715T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.2882T= MANE Select	ENSP00000347507.3:p.Leu961=
ENST00000355349.3:c.2882T=	ENSP00000347507.3:p.Leu961=
NM_000257.3:c.2882T=	NP_000248.2:p.Leu961=
XR_245686.3:n.2988T=
XM_017021340.1:c.2882T=	XP_016876829.1:p.Leu961=
NM_000257.4:c.2882T= MANE Select	NP_000248.2:p.Leu961=