Canonical Allele Identifier: CA937669348
Gene: MYBPC3 HGNC NCBI

Linked Data

dbSNP Id: rs2095884758

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47338431del , CM000673.2:g.47338431del GRCh38
NC_000011.9:g.47359982del , CM000673.1:g.47359982del GRCh37
NC_000011.8:g.47316558del NCBI36
NG_007667.1:g.19272del , LRG_386:g.19272del

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.2308+89del MANE Select ENSP00000442795.1:n.2308+89del
ENST00000256993.8:c.2308+89del ENSP00000256993.5:n.2308+89del
ENST00000399249.6:c.2308+89del ENSP00000382193.2:n.2308+89del
ENST00000544791.1:c.2308+89del ENSP00000444259.1:n.2308+89del
ENST00000545968.5:c.2308+89del ENSP00000442795.1:n.2308+89del
NM_000256.3:c.2308+89del , LRG_386t1:c.2308+89del MANE Select NP_000247.2:n.2308+89del
XM_011520117.1:c.2290+89del XP_011518419.1:n.2290+89del
XM_011520118.1:c.2227+89del XP_011518420.1:n.2227+89del