Canonical Allele Identifier: CA16042816
Gene: MYBPC3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372710
ClinVar RCV Id: RCV000412962
dbSNP Id: rs1057517939

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47351295dup , CM000673.2:g.47351295dup GRCh38
NC_000011.9:g.47372846dup , CM000673.1:g.47372846dup GRCh37
NC_000011.8:g.47329422dup NCBI36
NG_007667.1:g.6408dup , LRG_386:g.6408dup

Transcript Alleles

HGVS Amino-acid change
NM_000256.3:c.236dup , LRG_386t1:c.236dup
XM_011520117.1:c.236dup
XM_011520118.1:c.236dup
ENST00000256993.8:c.236dup
ENST00000399249.6:c.236dup
ENST00000544791.1:c.236dup
ENST00000545968.5:c.236dup