Canonical Allele Identifier: CA2123446213

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419937G= , CM000676.2:g.23419937G=	GRCh38
NC_000014.8:g.23889146G= , CM000676.1:g.23889146G=	GRCh37
NC_000014.7:g.22958986G=	NCBI36
NG_007884.1:g.20725C= , LRG_384:g.20725C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3634C= MANE Select	ENSP00000347507.3:p.Arg1212=
ENST00000355349.3:c.3634C=	ENSP00000347507.3:p.Arg1212=
NM_000257.3:c.3634C=	NP_000248.2:p.Arg1212=
XM_017021340.1:c.3634C=	XP_016876829.1:p.Arg1212=
NM_000257.4:c.3634C= MANE Select	NP_000248.2:p.Arg1212=