Canonical Allele Identifier: CA2123450271

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23422085C= , CM000676.2:g.23422085C=	GRCh38
NC_000014.8:g.23891294C= , CM000676.1:g.23891294C=	GRCh37
NC_000014.7:g.22961134C=	NCBI36
NG_007884.1:g.18577G= , LRG_384:g.18577G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.3245+95G= MANE Select	ENSP00000347507.3:n.3245+95G=
ENST00000355349.3:c.3245+95G=	ENSP00000347507.3:n.3245+95G=
NM_000257.3:c.3245+95G=	NP_000248.2:n.3245+95G=
XR_245686.3:n.3351+95G=
XM_017021340.1:c.3245+95G=	XP_016876829.1:n.3245+95G=
NM_000257.4:c.3245+95G= MANE Select	NP_000248.2:n.3245+95G=