Canonical Allele Identifier: CA2123459003

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23413968A= , CM000676.2:g.23413968A=	GRCh38
NC_000014.8:g.23883177A= , CM000676.1:g.23883177A=	GRCh37
NC_000014.7:g.22953017A=	NCBI36
NG_007884.1:g.26694T= , LRG_384:g.26694T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.5655+39T= MANE Select	ENSP00000347507.3:n.5655+39T=
ENST00000355349.3:c.5655+39T=	ENSP00000347507.3:n.5655+39T=
NM_000257.3:c.5655+39T=	NP_000248.2:n.5655+39T=
XM_017021340.1:c.5655+39T=	XP_016876829.1:n.5655+39T=
NM_000257.4:c.5655+39T= MANE Select	NP_000248.2:n.5655+39T=