Canonical Allele Identifier: CA599059913
Gene: MYBPC3 HGNC NCBI

Linked Data

dbSNP Id: rs1166892196

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47347803dup , CM000673.2:g.47347803dup GRCh38
NC_000011.9:g.47369354dup , CM000673.1:g.47369354dup GRCh37
NC_000011.8:g.47325930dup NCBI36
NG_007667.1:g.9901dup , LRG_386:g.9901dup

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.821+55dup MANE Select ENSP00000442795.1:n.821+55dup
ENST00000256993.8:c.821+55dup ENSP00000256993.5:n.821+55dup
ENST00000399249.6:c.821+55dup ENSP00000382193.2:n.821+55dup
ENST00000544791.1:c.821+55dup ENSP00000444259.1:n.821+55dup
ENST00000545968.5:c.821+55dup ENSP00000442795.1:n.821+55dup
NM_000256.3:c.821+55dup , LRG_386t1:c.821+55dup MANE Select NP_000247.2:n.821+55dup
XM_011520117.1:c.821+55dup XP_011518419.1:n.821+55dup
XM_011520118.1:c.821+55dup XP_011518420.1:n.821+55dup