Canonical Allele Identifier: CA2123445572

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419620A= , CM000676.2:g.23419620A=	GRCh38
NC_000014.8:g.23888829A= , CM000676.1:g.23888829A=	GRCh37
NC_000014.7:g.22958669A=	NCBI36
NG_007884.1:g.21042T= , LRG_384:g.21042T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3727-11T= MANE Select	ENSP00000347507.3:n.3727-11T=
ENST00000355349.3:c.3727-11T=	ENSP00000347507.3:n.3727-11T=
NM_000257.3:c.3727-11T=	NP_000248.2:n.3727-11T=
XM_017021340.1:c.3727-11T=	XP_016876829.1:n.3727-11T=
NM_000257.4:c.3727-11T= MANE Select	NP_000248.2:n.3727-11T=