Canonical Allele Identifier: CA380341658

Gene: MYBPC3

Linked Data

• ClinVar Variation Id: 920413
• ClinVar RCV Id: RCV001179168
• dbSNP Id: rs2095900637
• MyVariant Identifiers: chr11:g.47372846T>C (hg19) ; chr11:g.47351295T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47351295T>C , CM000673.2:g.47351295T>C	GRCh38
NC_000011.9:g.47372846T>C , CM000673.1:g.47372846T>C	GRCh37
NC_000011.8:g.47329422T>C	NCBI36
NG_007667.1:g.6408A>G , LRG_386:g.6408A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000545968.6:c.236A>G MANE Select	ENSP00000442795.1:p.Tyr79Cys
ENST00000256993.8:c.236A>G	ENSP00000256993.5:p.Tyr79Cys
ENST00000399249.6:c.236A>G	ENSP00000382193.2:p.Tyr79Cys
ENST00000544791.1:c.236A>G	ENSP00000444259.1:p.Tyr79Cys
ENST00000545968.5:c.236A>G	ENSP00000442795.1:p.Tyr79Cys
NM_000256.3:c.236A>G , LRG_386t1:c.236A>G MANE Select	NP_000247.2:p.Tyr79Cys
XM_011520117.1:c.236A>G	XP_011518419.1:p.Tyr79Cys
XM_011520118.1:c.236A>G	XP_011518420.1:p.Tyr79Cys