Canonical Allele Identifier: CA937666811
Gene: MYBPC3 HGNC NCBI

Linked Data

dbSNP Id: rs2095880712
gnomAD v3: 11-47334916-C-T
gnomAD v4: 11-47334916-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47334916C>T , CM000673.2:g.47334916C>T GRCh38
NC_000011.9:g.47356467C>T , CM000673.1:g.47356467C>T GRCh37
NC_000011.8:g.47313043C>T NCBI36
NG_007667.1:g.22787G>A , LRG_386:g.22787G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.2905+126G>A MANE Select ENSP00000442795.1:n.2905+126G>A
ENST00000256993.8:c.2905+126G>A ENSP00000256993.5:n.2905+126G>A
ENST00000399249.6:c.2905+126G>A ENSP00000382193.2:n.2905+126G>A
ENST00000545968.5:c.2905+126G>A ENSP00000442795.1:n.2905+126G>A
NM_000256.3:c.2905+126G>A , LRG_386t1:c.2905+126G>A MANE Select NP_000247.2:n.2905+126G>A
XM_011520117.1:c.2887+126G>A XP_011518419.1:n.2887+126G>A
XM_011520118.1:c.2824+126G>A XP_011518420.1:n.2824+126G>A
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