Canonical Allele Identifier: CA2123441859

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417858G= , CM000676.2:g.23417858G=	GRCh38
NC_000014.8:g.23887067G= , CM000676.1:g.23887067G=	GRCh37
NC_000014.7:g.22956907G=	NCBI36
NG_007884.1:g.22804C= , LRG_384:g.22804C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-172C= MANE Select	ENSP00000347507.3:n.4170-172C=
ENST00000355349.3:c.4170-172C=	ENSP00000347507.3:n.4170-172C=
NM_000257.3:c.4170-172C=	NP_000248.2:n.4170-172C=
XM_017021340.1:c.4170-172C=	XP_016876829.1:n.4170-172C=
NM_000257.4:c.4170-172C= MANE Select	NP_000248.2:n.4170-172C=