Canonical Allele Identifier: CA2123445676

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419665G= , CM000676.2:g.23419665G=	GRCh38
NC_000014.8:g.23888874G= , CM000676.1:g.23888874G=	GRCh37
NC_000014.7:g.22958714G=	NCBI36
NG_007884.1:g.20997C= , LRG_384:g.20997C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3727-56C= MANE Select	ENSP00000347507.3:n.3727-56C=
ENST00000355349.3:c.3727-56C=	ENSP00000347507.3:n.3727-56C=
NM_000257.3:c.3727-56C=	NP_000248.2:n.3727-56C=
XM_017021340.1:c.3727-56C=	XP_016876829.1:n.3727-56C=
NM_000257.4:c.3727-56C= MANE Select	NP_000248.2:n.3727-56C=