Canonical Allele Identifier: CA012096
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 42616
ClinVar RCV Id: RCV000035484
dbSNP Id: rs397515961
MyVariant Identifiers: chr11:g.47359342A>G (hg19) chr11:g.47337791A>G (hg38)
PubMed: PMID:16004897 PMID:18533079 PMID:21302287 PMID:23233322 PMID:23549607
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47337791A>G , CM000673.2:g.47337791A>G GRCh38
NC_000011.9:g.47359342A>G , CM000673.1:g.47359342A>G GRCh37
NC_000011.8:g.47315918A>G NCBI36
NG_007667.1:g.19912T>C , LRG_386:g.19912T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.2312T>C MANE Select ENSP00000442795.1:p.Val771Ala
ENST00000256993.8:c.2312T>C ENSP00000256993.5:p.Val771Ala
ENST00000399249.6:c.2312T>C ENSP00000382193.2:p.Val771Ala
ENST00000544791.1:c.2312T>C ENSP00000444259.1:p.Val771Ala
ENST00000545968.5:c.2312T>C ENSP00000442795.1:p.Val771Ala
NM_000256.3:c.2312T>C , LRG_386t1:c.2312T>C MANE Select NP_000247.2:p.Val771Ala
XM_011520117.1:c.2294T>C XP_011518419.1:p.Val765Ala
XM_011520118.1:c.2231T>C XP_011518420.1:p.Val744Ala
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