Canonical Allele Identifier: CA078094

Gene: MYBPC3

Linked Data

• dbSNP Id: rs750806768
• ExAC: 11:47364358 T / C
• gnomAD v2: 11-47364358-T-C
• gnomAD v3: 11-47342807-T-C
• gnomAD v4: 11-47342807-T-C
• MyVariant Identifiers: chr11:g.47364358T>C (hg19) ; chr11:g.47342807T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47342807T>C , CM000673.2:g.47342807T>C	GRCh38
NC_000011.9:g.47364358T>C , CM000673.1:g.47364358T>C	GRCh37
NC_000011.8:g.47320934T>C	NCBI36
NG_007667.1:g.14896A>G , LRG_386:g.14896A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1457+23A>G MANE Select	ENSP00000442795.1:n.1457+23A>G
ENST00000256993.8:c.1457+23A>G	ENSP00000256993.5:n.1457+23A>G
ENST00000399249.6:c.1457+23A>G	ENSP00000382193.2:n.1457+23A>G
ENST00000544791.1:c.1457+23A>G	ENSP00000444259.1:n.1457+23A>G
ENST00000545968.5:c.1457+23A>G	ENSP00000442795.1:n.1457+23A>G
NM_000256.3:c.1457+23A>G , LRG_386t1:c.1457+23A>G MANE Select	NP_000247.2:n.1457+23A>G
XM_011520117.1:c.1439+23A>G	XP_011518419.1:n.1439+23A>G
XM_011520118.1:c.1457+23A>G	XP_011518420.1:n.1457+23A>G