Canonical Allele Identifier: CA2123445576

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419624A= , CM000676.2:g.23419624A=	GRCh38
NC_000014.8:g.23888833A= , CM000676.1:g.23888833A=	GRCh37
NC_000014.7:g.22958673A=	NCBI36
NG_007884.1:g.21038T= , LRG_384:g.21038T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3727-15T= MANE Select	ENSP00000347507.3:n.3727-15T=
ENST00000355349.3:c.3727-15T=	ENSP00000347507.3:n.3727-15T=
NM_000257.3:c.3727-15T=	NP_000248.2:n.3727-15T=
XM_017021340.1:c.3727-15T=	XP_016876829.1:n.3727-15T=
NM_000257.4:c.3727-15T= MANE Select	NP_000248.2:n.3727-15T=