Canonical Allele Identifier: CA677012936

Gene: MYBPC3

Linked Data

• dbSNP Id: rs1390974432
• gnomAD v3: 11-47332046-A-C
• gnomAD v4: 11-47332046-A-C
• MyVariant Identifiers: chr11:g.47353597A>C (hg19) ; chr11:g.47332046A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47332046A>C , CM000673.2:g.47332046A>C	GRCh38
NC_000011.9:g.47353597A>C , CM000673.1:g.47353597A>C	GRCh37
NC_000011.8:g.47310173A>C	NCBI36
NG_007667.1:g.25657T>G , LRG_386:g.25657T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000545968.6:c.3814+26T>G MANE Select	ENSP00000442795.1:n.3814+26T>G
ENST00000256993.8:c.3814+26T>G	ENSP00000256993.5:n.3814+26T>G
ENST00000399249.6:c.3814+26T>G	ENSP00000382193.2:n.3814+26T>G
ENST00000545968.5:c.3814+26T>G	ENSP00000442795.1:n.3814+26T>G
NM_000256.3:c.3814+26T>G , LRG_386t1:c.3814+26T>G MANE Select	NP_000247.2:n.3814+26T>G
XM_011520117.1:c.3796+26T>G	XP_011518419.1:n.3796+26T>G
XM_011520118.1:c.3733+26T>G	XP_011518420.1:n.3733+26T>G