Canonical Allele Identifier: CA042951

Gene: MYBPC3

Linked Data

• ClinVar Variation Id: 219403
• ClinVar RCV Id: RCV000206400 ; RCV001184019 ; RCV002503799 ; RCV002345726 ; RCV003991469
• dbSNP Id: rs772073491
• ExAC: 11:47365113 C / T
• gnomAD v2: 11-47365113-C-T
• gnomAD v3: 11-47343562-C-T
• gnomAD v4: 11-47343562-C-T
• COSMIC: COSM927423 ; COSM4865075
• MyVariant Identifiers: chr11:g.47365113C>T (hg19) ; chr11:g.47343562C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47343562C>T , CM000673.2:g.47343562C>T	GRCh38
NC_000011.9:g.47365113C>T , CM000673.1:g.47365113C>T	GRCh37
NC_000011.8:g.47321689C>T	NCBI36
NG_007667.1:g.14141G>A , LRG_386:g.14141G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1153G>A MANE Select	ENSP00000442795.1:p.Val385Met
ENST00000256993.8:c.1153G>A	ENSP00000256993.5:p.Val385Met
ENST00000399249.6:c.1153G>A	ENSP00000382193.2:p.Val385Met
ENST00000544791.1:c.1153G>A	ENSP00000444259.1:p.Val385Met
ENST00000545968.5:c.1153G>A	ENSP00000442795.1:p.Val385Met
NM_000256.3:c.1153G>A , LRG_386t1:c.1153G>A MANE Select	NP_000247.2:p.Val385Met
XM_011520117.1:c.1135G>A	XP_011518419.1:p.Val379Met
XM_011520118.1:c.1153G>A	XP_011518420.1:p.Val385Met