Canonical Allele Identifier: CA1969336952
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47343256T= , CM000673.2:g.47343256T= GRCh38
NC_000011.9:g.47364807T= , CM000673.1:g.47364807T= GRCh37
NC_000011.8:g.47321383T= NCBI36
NG_007667.1:g.14447A= , LRG_386:g.14447A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.1226+4A= MANE Select ENSP00000442795.1:n.1226+4A=
ENST00000256993.8:c.1224-108A= ENSP00000256993.5:n.1224-108A=
ENST00000399249.6:c.1226+4A= ENSP00000382193.2:n.1226+4A=
ENST00000544791.1:c.1226+4A= ENSP00000444259.1:n.1226+4A=
ENST00000545968.5:c.1226+4A= ENSP00000442795.1:n.1226+4A=
NM_000256.3:c.1226+4A= , LRG_386t1:c.1226+4A= MANE Select NP_000247.2:n.1226+4A=
XM_011520117.1:c.1208+4A= XP_011518419.1:n.1208+4A=
XM_011520118.1:c.1226+4A= XP_011518420.1:n.1226+4A=