Canonical Allele Identifier: CA013994
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 177675
dbSNP Id: rs730880335

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47350575dup , CM000673.2:g.47350575dup GRCh38
NC_000011.9:g.47372126dup , CM000673.1:g.47372126dup GRCh37
NC_000011.8:g.47328702dup NCBI36
NG_007667.1:g.7128dup , LRG_386:g.7128dup

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.333dup MANE Select ENSP00000442795.1:p.Glu112Ter
ENST00000256993.8:c.333dup ENSP00000256993.5:p.Glu112Ter
ENST00000399249.6:c.333dup ENSP00000382193.2:p.Glu112Ter
ENST00000544791.1:c.333dup ENSP00000444259.1:p.Glu112Ter
ENST00000545968.5:c.333dup ENSP00000442795.1:p.Glu112Ter
NM_000256.3:c.333dup , LRG_386t1:c.333dup MANE Select NP_000247.2:p.Glu112Ter
XM_011520117.1:c.333dup XP_011518419.1:p.Glu112Ter
XM_011520118.1:c.333dup XP_011518420.1:p.Glu112Ter