Canonical Allele Identifier: CA380331037
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230864
ClinVar RCV Id: RCV004522978
dbSNP Id: rs1476576625

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47346228G>A , CM000673.2:g.47346228G>A GRCh38
NC_000011.9:g.47367779G>A , CM000673.1:g.47367779G>A GRCh37
NC_000011.8:g.47324355G>A NCBI36
NG_007667.1:g.11475C>T , LRG_386:g.11475C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.1069C>T MANE Select ENSP00000442795.1:p.Arg357Cys
ENST00000256993.8:c.1069C>T ENSP00000256993.5:p.Arg357Cys
ENST00000399249.6:c.1069C>T ENSP00000382193.2:p.Arg357Cys
ENST00000544791.1:c.1069C>T ENSP00000444259.1:p.Arg357Cys
ENST00000545968.5:c.1069C>T ENSP00000442795.1:p.Arg357Cys
NM_000256.3:c.1069C>T , LRG_386t1:c.1069C>T MANE Select NP_000247.2:p.Arg357Cys
XM_011520117.1:c.1051C>T XP_011518419.1:p.Arg351Cys
XM_011520118.1:c.1069C>T XP_011518420.1:p.Arg357Cys