Canonical Allele Identifier: CA010705

Gene: MYBPC3

Linked Data

• ClinVar Variation Id: 180944
• ClinVar RCV Id: RCV000158102 ; RCV001857559
• dbSNP Id: rs730880547
• gnomAD v4: 11-47342607-C-A
• MyVariant Identifiers: chr11:g.47364158C>A (hg19) ; chr11:g.47342607C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47342607C>A , CM000673.2:g.47342607C>A	GRCh38
NC_000011.9:g.47364158C>A , CM000673.1:g.47364158C>A	GRCh37
NC_000011.8:g.47320734C>A	NCBI36
NG_007667.1:g.15096G>T , LRG_386:g.15096G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1595G>T MANE Select	ENSP00000442795.1:p.Gly532Val
ENST00000256993.8:c.1595G>T	ENSP00000256993.5:p.Gly532Val
ENST00000399249.6:c.1595G>T	ENSP00000382193.2:p.Gly532Val
ENST00000544791.1:c.1595G>T	ENSP00000444259.1:p.Gly532Val
ENST00000545968.5:c.1595G>T	ENSP00000442795.1:p.Gly532Val
NM_000256.3:c.1595G>T , LRG_386t1:c.1595G>T MANE Select	NP_000247.2:p.Gly532Val
XM_011520117.1:c.1577G>T	XP_011518419.1:p.Gly526Val
XM_011520118.1:c.1595G>T	XP_011518420.1:p.Gly532Val