Canonical Allele Identifier: CA919376104

Gene: MYH7

Linked Data

• dbSNP Id: rs1555338586

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431019del , CM000676.2:g.23431019del	GRCh38
NC_000014.8:g.23900228del , CM000676.1:g.23900228del	GRCh37
NC_000014.7:g.22970068del	NCBI36
NG_007884.1:g.9644del , LRG_384:g.9644del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.797-19del MANE Select	ENSP00000347507.3:n.797-19del
ENST00000355349.3:c.797-19del	ENSP00000347507.3:n.797-19del
NM_000257.3:c.797-19del	NP_000248.2:n.797-19del
XR_245686.3:n.903-19del
XM_017021340.1:c.797-19del	XP_016876829.1:n.797-19del
NM_000257.4:c.797-19del MANE Select	NP_000248.2:n.797-19del