Canonical Allele Identifier: CA380324327

Gene: MYBPC3

Linked Data

• ClinVar Variation Id: 3069854
• ClinVar RCV Id: RCV004009886
• gnomAD v4: 11-47342073-C-T
• MyVariant Identifiers: chr11:g.47363624C>T (hg19) ; chr11:g.47342073C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47342073C>T , CM000673.2:g.47342073C>T	GRCh38
NC_000011.9:g.47363624C>T , CM000673.1:g.47363624C>T	GRCh37
NC_000011.8:g.47320200C>T	NCBI36
NG_007667.1:g.15630G>A , LRG_386:g.15630G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1708G>A MANE Select	ENSP00000442795.1:p.Asp570Asn
ENST00000256993.8:c.1708G>A	ENSP00000256993.5:p.Asp570Asn
ENST00000399249.6:c.1708G>A	ENSP00000382193.2:p.Asp570Asn
ENST00000544791.1:c.1708G>A	ENSP00000444259.1:p.Asp570Asn
ENST00000545968.5:c.1708G>A	ENSP00000442795.1:p.Asp570Asn
NM_000256.3:c.1708G>A , LRG_386t1:c.1708G>A MANE Select	NP_000247.2:p.Asp570Asn
XM_011520117.1:c.1690G>A	XP_011518419.1:p.Asp564Asn
XM_011520118.1:c.1708G>A	XP_011518420.1:p.Asp570Asn