Canonical Allele Identifier: CA913187679
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076026
ClinVar RCV Id: RCV004018344

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47333753dup , CM000673.2:g.47333753dup GRCh38
NC_000011.9:g.47355304dup , CM000673.1:g.47355304dup GRCh37
NC_000011.8:g.47311880dup NCBI36
NG_007667.1:g.23952dup , LRG_386:g.23952dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.2996dup
ENST00000256993.8:c.2996dup
ENST00000399249.6:c.2996dup
ENST00000545968.5:c.2996dup
NM_000256.3:c.2996dup , LRG_386t1:c.2996dup
XM_011520117.1:c.2978dup
XM_011520118.1:c.2915dup