Canonical Allele Identifier: CA1969336152
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47342811C= , CM000673.2:g.47342811C= GRCh38
NC_000011.9:g.47364362C= , CM000673.1:g.47364362C= GRCh37
NC_000011.8:g.47320938C= NCBI36
NG_007667.1:g.14892G= , LRG_386:g.14892G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.1457+19G= MANE Select ENSP00000442795.1:n.1457+19G=
ENST00000256993.8:c.1457+19G= ENSP00000256993.5:n.1457+19G=
ENST00000399249.6:c.1457+19G= ENSP00000382193.2:n.1457+19G=
ENST00000544791.1:c.1457+19G= ENSP00000444259.1:n.1457+19G=
ENST00000545968.5:c.1457+19G= ENSP00000442795.1:n.1457+19G=
NM_000256.3:c.1457+19G= , LRG_386t1:c.1457+19G= MANE Select NP_000247.2:n.1457+19G=
XM_011520117.1:c.1439+19G= XP_011518419.1:n.1439+19G=
XM_011520118.1:c.1457+19G= XP_011518420.1:n.1457+19G=