Canonical Allele Identifier: CA10586355

Gene: MYBPC3

Linked Data

• ClinVar Variation Id: 254155
• ClinVar RCV Id: RCV000240632 ; RCV000768467
• dbSNP Id: rs886037902
• MyVariant Identifiers: chr11:g.47367920_47367921del (hg19) ; chr11:g.47346369_47346370del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47346370_47346371del , CM000673.2:g.47346370_47346371del	GRCh38
NC_000011.9:g.47367921_47367922del , CM000673.1:g.47367921_47367922del	GRCh37
NC_000011.8:g.47324497_47324498del	NCBI36
NG_007667.1:g.11333_11334del , LRG_386:g.11333_11334del

Transcript Alleles

HGVS	Amino-acid change
ENST00000545968.6:c.927_928del
ENST00000256993.8:c.927_928del
ENST00000399249.6:c.927_928del
ENST00000544791.1:c.927_928del
ENST00000545968.5:c.927_928del
NM_000256.3:c.927_928del , LRG_386t1:c.927_928del
XM_011520117.1:c.909_910del
XM_011520118.1:c.927_928del