Canonical Allele Identifier: CA2123446800

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420100C= , CM000676.2:g.23420100C=	GRCh38
NC_000014.8:g.23889309C= , CM000676.1:g.23889309C=	GRCh37
NC_000014.7:g.22959149C=	NCBI36
NG_007884.1:g.20562G= , LRG_384:g.20562G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3471G= MANE Select	ENSP00000347507.3:p.Thr1157=
ENST00000355349.3:c.3471G=	ENSP00000347507.3:p.Thr1157=
NM_000257.3:c.3471G=	NP_000248.2:p.Thr1157=
XM_017021340.1:c.3471G=	XP_016876829.1:p.Thr1157=
NM_000257.4:c.3471G= MANE Select	NP_000248.2:p.Thr1157=