Canonical Allele Identifier: CA1969332149
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789115
dbSNP Id: rs2095884867

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47338517_47338537del , CM000673.2:g.47338517_47338537del GRCh38
NC_000011.9:g.47360068_47360088del , CM000673.1:g.47360068_47360088del GRCh37
NC_000011.8:g.47316644_47316664del NCBI36
NG_007667.1:g.19166_19186del , LRG_386:g.19166_19186del

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.2291_2308+3del
ENST00000256993.8:c.2291_2308+3del
ENST00000399249.6:c.2291_2308+3del
ENST00000544791.1:c.2291_2308+3del
ENST00000545968.5:c.2291_2308+3del
NM_000256.3:c.2291_2308+3del , LRG_386t1:c.2291_2308+3del
XM_011520117.1:c.2273_2290+3del
XM_011520118.1:c.2210_2227+3del