Canonical Allele Identifier: CA2123452654

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423415C= , CM000676.2:g.23423415C=	GRCh38
NC_000014.8:g.23892624C= , CM000676.1:g.23892624C=	GRCh37
NC_000014.7:g.22962464C=	NCBI36
NG_007884.1:g.17247G= , LRG_384:g.17247G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+132G= MANE Select	ENSP00000347507.3:n.3099+132G=
ENST00000355349.3:c.3099+132G=	ENSP00000347507.3:n.3099+132G=
NM_000257.3:c.3099+132G=	NP_000248.2:n.3099+132G=
XR_245686.3:n.3205+132G=
XM_017021340.1:c.3099+132G=	XP_016876829.1:n.3099+132G=
NM_000257.4:c.3099+132G= MANE Select	NP_000248.2:n.3099+132G=