Canonical Allele Identifier: CA2123441871

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417868C= , CM000676.2:g.23417868C=	GRCh38
NC_000014.8:g.23887077C= , CM000676.1:g.23887077C=	GRCh37
NC_000014.7:g.22956917C=	NCBI36
NG_007884.1:g.22794G= , LRG_384:g.22794G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-182G= MANE Select	ENSP00000347507.3:n.4170-182G=
ENST00000355349.3:c.4170-182G=	ENSP00000347507.3:n.4170-182G=
NM_000257.3:c.4170-182G=	NP_000248.2:n.4170-182G=
XM_017021340.1:c.4170-182G=	XP_016876829.1:n.4170-182G=
NM_000257.4:c.4170-182G= MANE Select	NP_000248.2:n.4170-182G=