Canonical Allele Identifier: CA1969335947
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47333725T= , CM000673.2:g.47333725T= GRCh38
NC_000011.9:g.47355276T= , CM000673.1:g.47355276T= GRCh37
NC_000011.8:g.47311852T= NCBI36
NG_007667.1:g.23978A= , LRG_386:g.23978A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.3022A= MANE Select ENSP00000442795.1:p.Thr1008=
ENST00000256993.8:c.3022A= ENSP00000256993.5:p.Thr1008=
ENST00000399249.6:c.3022A= ENSP00000382193.2:p.Thr1008=
ENST00000545968.5:c.3022A= ENSP00000442795.1:p.Thr1008=
NM_000256.3:c.3022A= , LRG_386t1:c.3022A= MANE Select NP_000247.2:p.Thr1008=
XM_011520117.1:c.3004A= XP_011518419.1:p.Thr1002=
XM_011520118.1:c.2941A= XP_011518420.1:p.Thr981=