Canonical Allele Identifier: CA2123442361

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23418181A= , CM000676.2:g.23418181A=	GRCh38
NC_000014.8:g.23887390A= , CM000676.1:g.23887390A=	GRCh37
NC_000014.7:g.22957230A=	NCBI36
NG_007884.1:g.22481T= , LRG_384:g.22481T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.4169+29T= MANE Select	ENSP00000347507.3:n.4169+29T=
ENST00000355349.3:c.4169+29T=	ENSP00000347507.3:n.4169+29T=
NM_000257.3:c.4169+29T=	NP_000248.2:n.4169+29T=
XM_017021340.1:c.4169+29T=	XP_016876829.1:n.4169+29T=
NM_000257.4:c.4169+29T= MANE Select	NP_000248.2:n.4169+29T=