Canonical Allele Identifier: CA10645070

Gene: MYH7

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23429768C>T , CM000676.2:g.23429768C>T	GRCh38
NC_000014.8:g.23898977C>T , CM000676.1:g.23898977C>T	GRCh37
NC_000014.7:g.22968817C>T	NCBI36
NG_007884.1:g.10894G>A , LRG_384:g.10894G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.1138+7G>A MANE Select	ENSP00000347507.3:n.1138+7G>A
ENST00000355349.3:c.1138+7G>A	ENSP00000347507.3:n.1138+7G>A
NM_000257.3:c.1138+7G>A	NP_000248.2:n.1138+7G>A
XR_245686.3:n.1244+7G>A
XM_017021340.1:c.1138+7G>A	XP_016876829.1:n.1138+7G>A
NM_000257.4:c.1138+7G>A MANE Select	NP_000248.2:n.1138+7G>A