Canonical Allele Identifier: CA2580084155
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2121766
ClinVar RCV Id: RCV003049323

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47338502_47338530del , CM000673.2:g.47338502_47338530del GRCh38
NC_000011.9:g.47360053_47360081del , CM000673.1:g.47360053_47360081del GRCh37
NC_000011.8:g.47316629_47316657del NCBI36
NG_007667.1:g.19177_19205del , LRG_386:g.19177_19205del

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.2302_2308+22del
ENST00000256993.8:c.2302_2308+22del
ENST00000399249.6:c.2302_2308+22del
ENST00000544791.1:c.2302_2308+22del
ENST00000545968.5:c.2302_2308+22del
NM_000256.3:c.2302_2308+22del , LRG_386t1:c.2302_2308+22del
XM_011520117.1:c.2284_2290+22del
XM_011520118.1:c.2221_2227+22del