Canonical Allele Identifier: CA10639339

Gene: MYBPC3

Linked Data

• ClinVar Variation Id: 304957
• ClinVar RCV Id: RCV000301384 ; RCV000358397 ; RCV000394792
• dbSNP Id: rs886048379
• MyVariant Identifiers: chr11:g.47364304G>A (hg19) ; chr11:g.47342753G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47342753G>A , CM000673.2:g.47342753G>A	GRCh38
NC_000011.9:g.47364304G>A , CM000673.1:g.47364304G>A	GRCh37
NC_000011.8:g.47320880G>A	NCBI36
NG_007667.1:g.14950C>T , LRG_386:g.14950C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000545968.6:c.1458-9C>T MANE Select	ENSP00000442795.1:n.1458-9C>T
ENST00000256993.8:c.1458-9C>T	ENSP00000256993.5:n.1458-9C>T
ENST00000399249.6:c.1458-9C>T	ENSP00000382193.2:n.1458-9C>T
ENST00000544791.1:c.1458-9C>T	ENSP00000444259.1:n.1458-9C>T
ENST00000545968.5:c.1458-9C>T	ENSP00000442795.1:n.1458-9C>T
NM_000256.3:c.1458-9C>T , LRG_386t1:c.1458-9C>T MANE Select	NP_000247.2:n.1458-9C>T
XM_011520117.1:c.1440-9C>T	XP_011518419.1:n.1440-9C>T
XM_011520118.1:c.1458-9C>T	XP_011518420.1:n.1458-9C>T