Canonical Allele Identifier: CA221695340

Gene: MYBPC3

Linked Data

• dbSNP Id: rs973061457
• gnomAD v2: 11-47363969-C-T
• gnomAD v3: 11-47342418-C-T
• gnomAD v4: 11-47342418-C-T
• MyVariant Identifiers: chr11:g.47363969C>T (hg19) ; chr11:g.47342418C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47342418C>T , CM000673.2:g.47342418C>T	GRCh38
NC_000011.9:g.47363969C>T , CM000673.1:g.47363969C>T	GRCh37
NC_000011.8:g.47320545C>T	NCBI36
NG_007667.1:g.15285G>A , LRG_386:g.15285G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000545968.6:c.1624+160G>A MANE Select	ENSP00000442795.1:n.1624+160G>A
ENST00000256993.8:c.1624+160G>A	ENSP00000256993.5:n.1624+160G>A
ENST00000399249.6:c.1624+160G>A	ENSP00000382193.2:n.1624+160G>A
ENST00000544791.1:c.1624+160G>A	ENSP00000444259.1:n.1624+160G>A
ENST00000545968.5:c.1624+160G>A	ENSP00000442795.1:n.1624+160G>A
NM_000256.3:c.1624+160G>A , LRG_386t1:c.1624+160G>A MANE Select	NP_000247.2:n.1624+160G>A
XM_011520117.1:c.1606+160G>A	XP_011518419.1:n.1606+160G>A
XM_011520118.1:c.1624+160G>A	XP_011518420.1:n.1624+160G>A