Canonical Allele Identifier: CA2499220965
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1074099
ClinVar RCV Id: RCV001387279
dbSNP Id: rs2142853045

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47335210del , CM000673.2:g.47335210del GRCh38
NC_000011.9:g.47356761del , CM000673.1:g.47356761del GRCh37
NC_000011.8:g.47313337del NCBI36
NG_007667.1:g.22494del , LRG_386:g.22494del

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.2738del
ENST00000256993.8:c.2738del
ENST00000399249.6:c.2738del
ENST00000545968.5:c.2738del
NM_000256.3:c.2738del , LRG_386t1:c.2738del
XM_011520117.1:c.2720del
XM_011520118.1:c.2657del