Canonical Allele Identifier: CA2123456199

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433759G= , CM000676.2:g.23433759G=	GRCh38
NC_000014.8:g.23902968G= , CM000676.1:g.23902968G=	GRCh37
NC_000014.7:g.22972808G=	NCBI36
NG_007884.1:g.6903C= , LRG_384:g.6903C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.-8-19C= MANE Select	ENSP00000347507.3:n.-8-19C=
ENST00000355349.3:c.-8-19C=	ENSP00000347507.3:n.-8-19C=
NM_000257.3:c.-8-19C=	NP_000248.2:n.-8-19C=
XR_245686.3:n.99-19C=
XM_017021340.1:c.-8-19C=	XP_016876829.1:n.-8-19C=
NM_000257.4:c.-8-19C= MANE Select	NP_000248.2:n.-8-19C=