Canonical Allele Identifier: CA2123445613

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419636T= , CM000676.2:g.23419636T=	GRCh38
NC_000014.8:g.23888845T= , CM000676.1:g.23888845T=	GRCh37
NC_000014.7:g.22958685T=	NCBI36
NG_007884.1:g.21026A= , LRG_384:g.21026A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3727-27A= MANE Select	ENSP00000347507.3:n.3727-27A=
ENST00000355349.3:c.3727-27A=	ENSP00000347507.3:n.3727-27A=
NM_000257.3:c.3727-27A=	NP_000248.2:n.3727-27A=
XM_017021340.1:c.3727-27A=	XP_016876829.1:n.3727-27A=
NM_000257.4:c.3727-27A= MANE Select	NP_000248.2:n.3727-27A=