Canonical Allele Identifier: CA1969336938
Gene: MYBPC3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47343232A= , CM000673.2:g.47343232A= GRCh38
NC_000011.9:g.47364783A= , CM000673.1:g.47364783A= GRCh37
NC_000011.8:g.47321359A= NCBI36
NG_007667.1:g.14471T= , LRG_386:g.14471T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.1226+28T= MANE Select ENSP00000442795.1:n.1226+28T=
ENST00000256993.8:c.1224-84T= ENSP00000256993.5:n.1224-84T=
ENST00000399249.6:c.1226+28T= ENSP00000382193.2:n.1226+28T=
ENST00000544791.1:c.1226+28T= ENSP00000444259.1:n.1226+28T=
ENST00000545968.5:c.1226+28T= ENSP00000442795.1:n.1226+28T=
NM_000256.3:c.1226+28T= , LRG_386t1:c.1226+28T= MANE Select NP_000247.2:n.1226+28T=
XM_011520117.1:c.1208+28T= XP_011518419.1:n.1208+28T=
XM_011520118.1:c.1226+28T= XP_011518420.1:n.1226+28T=
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