Canonical Allele Identifier: CA2123452063

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431603G= , CM000676.2:g.23431603G=	GRCh38
NC_000014.8:g.23900812G= , CM000676.1:g.23900812G=	GRCh37
NC_000014.7:g.22970652G=	NCBI36
NG_007884.1:g.9059C= , LRG_384:g.9059C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.714C= MANE Select	ENSP00000347507.3:p.Asn238=
ENST00000355349.3:c.714C=	ENSP00000347507.3:p.Asn238=
NM_000257.3:c.714C=	NP_000248.2:p.Asn238=
XR_245686.3:n.820C=
XM_017021340.1:c.714C=	XP_016876829.1:p.Asn238=
NM_000257.4:c.714C= MANE Select	NP_000248.2:p.Asn238=