Canonical Allele Identifier: CA078224

Gene: MYBPC3

Linked Data

• dbSNP Id: rs773894147
• ExAC: 11:47364108 T / A
• gnomAD v2: 11-47364108-T-A
• gnomAD v3: 11-47342557-T-A
• gnomAD v4: 11-47342557-T-A
• MyVariant Identifiers: chr11:g.47364108T>A (hg19) ; chr11:g.47342557T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47342557T>A , CM000673.2:g.47342557T>A	GRCh38
NC_000011.9:g.47364108T>A , CM000673.1:g.47364108T>A	GRCh37
NC_000011.8:g.47320684T>A	NCBI36
NG_007667.1:g.15146A>T , LRG_386:g.15146A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1624+21A>T MANE Select	ENSP00000442795.1:n.1624+21A>T
ENST00000256993.8:c.1624+21A>T	ENSP00000256993.5:n.1624+21A>T
ENST00000399249.6:c.1624+21A>T	ENSP00000382193.2:n.1624+21A>T
ENST00000544791.1:c.1624+21A>T	ENSP00000444259.1:n.1624+21A>T
ENST00000545968.5:c.1624+21A>T	ENSP00000442795.1:n.1624+21A>T
NM_000256.3:c.1624+21A>T , LRG_386t1:c.1624+21A>T MANE Select	NP_000247.2:n.1624+21A>T
XM_011520117.1:c.1606+21A>T	XP_011518419.1:n.1606+21A>T
XM_011520118.1:c.1624+21A>T	XP_011518420.1:n.1624+21A>T