Canonical Allele Identifier: CA079496
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 626757
ClinVar RCV Id: RCV000770319 RCV002533959
dbSNP Id: rs372821359
ExAC: 11:47353769 T / C
gnomAD v2: 11-47353769-T-C
gnomAD v4: 11-47332218-T-C
MyVariant Identifiers: chr11:g.47353769T>C (hg19) chr11:g.47332218T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47332218T>C , CM000673.2:g.47332218T>C GRCh38
NC_000011.9:g.47353769T>C , CM000673.1:g.47353769T>C GRCh37
NC_000011.8:g.47310345T>C NCBI36
NG_007667.1:g.25485A>G , LRG_386:g.25485A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.3668A>G MANE Select ENSP00000442795.1:p.Glu1223Gly
ENST00000256993.8:c.3668A>G ENSP00000256993.5:p.Glu1223Gly
ENST00000399249.6:c.3668A>G ENSP00000382193.2:p.Glu1223Gly
ENST00000545968.5:c.3668A>G ENSP00000442795.1:p.Glu1223Gly
NM_000256.3:c.3668A>G , LRG_386t1:c.3668A>G MANE Select NP_000247.2:p.Glu1223Gly
XM_011520117.1:c.3650A>G XP_011518419.1:p.Glu1217Gly
XM_011520118.1:c.3587A>G XP_011518420.1:p.Glu1196Gly
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