Canonical Allele Identifier: CA10638736
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 304958
ClinVar RCV Id: RCV000269773 RCV000365569 RCV003165828
dbSNP Id: rs886048380
gnomAD v3: 11-47343602-C-T
gnomAD v4: 11-47343602-C-T
MyVariant Identifiers: chr11:g.47365153C>T (hg19) chr11:g.47343602C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47343602C>T , CM000673.2:g.47343602C>T GRCh38
NC_000011.9:g.47365153C>T , CM000673.1:g.47365153C>T GRCh37
NC_000011.8:g.47321729C>T NCBI36
NG_007667.1:g.14101G>A , LRG_386:g.14101G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.1113G>A MANE Select ENSP00000442795.1:p.Pro371=
ENST00000256993.8:c.1113G>A ENSP00000256993.5:p.Pro371=
ENST00000399249.6:c.1113G>A ENSP00000382193.2:p.Pro371=
ENST00000544791.1:c.1113G>A ENSP00000444259.1:p.Pro371=
ENST00000545968.5:c.1113G>A ENSP00000442795.1:p.Pro371=
NM_000256.3:c.1113G>A , LRG_386t1:c.1113G>A MANE Select NP_000247.2:p.Pro371=
XM_011520117.1:c.1095G>A XP_011518419.1:p.Pro365=
XM_011520118.1:c.1113G>A XP_011518420.1:p.Pro371=
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