Canonical Allele Identifier: CA014855
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 181024
ClinVar RCV Id: RCV000158263
dbSNP Id: rs730880605

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47332111G>A , CM000673.2:g.47332111G>A GRCh38
NC_000011.9:g.47353662G>A , CM000673.1:g.47353662G>A GRCh37
NC_000011.8:g.47310238G>A NCBI36
NG_007667.1:g.25592C>T , LRG_386:g.25592C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.3775C>T MANE Select ENSP00000442795.1:p.Gln1259Ter
ENST00000256993.8:c.3775C>T ENSP00000256993.5:p.Gln1259Ter
ENST00000399249.6:c.3775C>T ENSP00000382193.2:p.Gln1259Ter
ENST00000545968.5:c.3775C>T ENSP00000442795.1:p.Gln1259Ter
NM_000256.3:c.3775C>T , LRG_386t1:c.3775C>T MANE Select NP_000247.2:p.Gln1259Ter
XM_011520117.1:c.3757C>T XP_011518419.1:p.Gln1253Ter
XM_011520118.1:c.3694C>T XP_011518420.1:p.Gln1232Ter