Canonical Allele Identifier: CA676997199

Gene: MYBPC3

Linked Data

• dbSNP Id: rs1451943762
• MyVariant Identifiers: chr11:g.47361160del (hg19) ; chr11:g.47339609del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47339611del , CM000673.2:g.47339611del	GRCh38
NC_000011.9:g.47361162del , CM000673.1:g.47361162del	GRCh37
NC_000011.8:g.47317738del	NCBI36
NG_007667.1:g.18094del , LRG_386:g.18094del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.2067+42del MANE Select	ENSP00000442795.1:n.2067+42del
ENST00000256993.8:c.2067+42del	ENSP00000256993.5:n.2067+42del
ENST00000399249.6:c.2067+42del	ENSP00000382193.2:n.2067+42del
ENST00000544791.1:c.2067+42del	ENSP00000444259.1:n.2067+42del
ENST00000545968.5:c.2067+42del	ENSP00000442795.1:n.2067+42del
NM_000256.3:c.2067+42del , LRG_386t1:c.2067+42del MANE Select	NP_000247.2:n.2067+42del
XM_011520117.1:c.2049+42del	XP_011518419.1:n.2049+42del
XM_011520118.1:c.2067+42del	XP_011518420.1:n.2067+42del