Canonical Allele Identifier: CA2123441358

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23427572A= , CM000676.2:g.23427572A=	GRCh38
NC_000014.8:g.23896781A= , CM000676.1:g.23896781A=	GRCh37
NC_000014.7:g.22966621A=	NCBI36
NG_007884.1:g.13090T= , LRG_384:g.13090T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.1888+13T= MANE Select	ENSP00000347507.3:n.1888+13T=
ENST00000355349.3:c.1888+13T=	ENSP00000347507.3:n.1888+13T=
NM_000257.3:c.1888+13T=	NP_000248.2:n.1888+13T=
XR_245686.3:n.1994+13T=
XM_017021340.1:c.1888+13T=	XP_016876829.1:n.1888+13T=
NM_000257.4:c.1888+13T= MANE Select	NP_000248.2:n.1888+13T=