Canonical Allele Identifier: CA2123450529

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23422203C= , CM000676.2:g.23422203C=	GRCh38
NC_000014.8:g.23891412C= , CM000676.1:g.23891412C=	GRCh37
NC_000014.7:g.22961252C=	NCBI36
NG_007884.1:g.18459G= , LRG_384:g.18459G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.3222G= MANE Select	ENSP00000347507.3:p.Gln1074=
ENST00000355349.3:c.3222G=	ENSP00000347507.3:p.Gln1074=
NM_000257.3:c.3222G=	NP_000248.2:p.Gln1074=
XR_245686.3:n.3328G=
XM_017021340.1:c.3222G=	XP_016876829.1:p.Gln1074=
NM_000257.4:c.3222G= MANE Select	NP_000248.2:p.Gln1074=