Canonical Allele Identifier: CA2123447583

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420346A= , CM000676.2:g.23420346A=	GRCh38
NC_000014.8:g.23889555A= , CM000676.1:g.23889555A=	GRCh37
NC_000014.7:g.22959395A=	NCBI36
NG_007884.1:g.20316T= , LRG_384:g.20316T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3337-112T= MANE Select	ENSP00000347507.3:n.3337-112T=
ENST00000355349.3:c.3337-112T=	ENSP00000347507.3:n.3337-112T=
NM_000257.3:c.3337-112T=	NP_000248.2:n.3337-112T=
XR_245686.3:n.3445-112T=
XM_017021340.1:c.3337-112T=	XP_016876829.1:n.3337-112T=
NM_000257.4:c.3337-112T= MANE Select	NP_000248.2:n.3337-112T=