Canonical Allele Identifier: CA2123441796

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417818T= , CM000676.2:g.23417818T=	GRCh38
NC_000014.8:g.23887027T= , CM000676.1:g.23887027T=	GRCh37
NC_000014.7:g.22956867T=	NCBI36
NG_007884.1:g.22844A= , LRG_384:g.22844A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-132A= MANE Select	ENSP00000347507.3:n.4170-132A=
ENST00000355349.3:c.4170-132A=	ENSP00000347507.3:n.4170-132A=
NM_000257.3:c.4170-132A=	NP_000248.2:n.4170-132A=
XM_017021340.1:c.4170-132A=	XP_016876829.1:n.4170-132A=
NM_000257.4:c.4170-132A= MANE Select	NP_000248.2:n.4170-132A=