Canonical Allele Identifier: CA2123447552

Gene: MYH7

Linked Data

• dbSNP Id: rs1892428021

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420323del , CM000676.2:g.23420323del	GRCh38
NC_000014.8:g.23889532del , CM000676.1:g.23889532del	GRCh37
NC_000014.7:g.22959372del	NCBI36
NG_007884.1:g.20339del , LRG_384:g.20339del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3337-89del MANE Select	ENSP00000347507.3:n.3337-89del
ENST00000355349.3:c.3337-89del	ENSP00000347507.3:n.3337-89del
NM_000257.3:c.3337-89del	NP_000248.2:n.3337-89del
XR_245686.3:n.3445-89del
XM_017021340.1:c.3337-89del	XP_016876829.1:n.3337-89del
NM_000257.4:c.3337-89del MANE Select	NP_000248.2:n.3337-89del