Canonical Allele Identifier: CA2123461943

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23415098A= , CM000676.2:g.23415098A=	GRCh38
NC_000014.8:g.23884307A= , CM000676.1:g.23884307A=	GRCh37
NC_000014.7:g.22954147A=	NCBI36
NG_007884.1:g.25564T= , LRG_384:g.25564T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.5456T= MANE Select	ENSP00000347507.3:p.Val1819=
ENST00000355349.3:c.5456T=	ENSP00000347507.3:p.Val1819=
NM_000257.3:c.5456T=	NP_000248.2:p.Val1819=
XM_017021340.1:c.5456T=	XP_016876829.1:p.Val1819=
NM_000257.4:c.5456T= MANE Select	NP_000248.2:p.Val1819=