Canonical Allele Identifier: CA919376098

Gene: MYH7

Linked Data

• dbSNP Id: rs869208102

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431017_23431018dup , CM000676.2:g.23431017_23431018dup	GRCh38
NC_000014.8:g.23900226_23900227dup , CM000676.1:g.23900226_23900227dup	GRCh37
NC_000014.7:g.22970066_22970067dup	NCBI36
NG_007884.1:g.9646_9647dup , LRG_384:g.9646_9647dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.797-17_797-16dup MANE Select	ENSP00000347507.3:n.797-17_797-16dup
ENST00000355349.3:c.797-17_797-16dup	ENSP00000347507.3:n.797-17_797-16dup
NM_000257.3:c.797-17_797-16dup	NP_000248.2:n.797-17_797-16dup
XR_245686.3:n.903-17_903-16dup
XM_017021340.1:c.797-17_797-16dup	XP_016876829.1:n.797-17_797-16dup
NM_000257.4:c.797-17_797-16dup MANE Select	NP_000248.2:n.797-17_797-16dup