Canonical Allele Identifier: CA380321423

Gene: MYBPC3

Linked Data

• gnomAD v4: 11-47339674-T-C
• MyVariant Identifiers: chr11:g.47361225T>C (hg19) ; chr11:g.47339674T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47339674T>C , CM000673.2:g.47339674T>C	GRCh38
NC_000011.9:g.47361225T>C , CM000673.1:g.47361225T>C	GRCh37
NC_000011.8:g.47317801T>C	NCBI36
NG_007667.1:g.18029A>G , LRG_386:g.18029A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.2044A>G MANE Select	ENSP00000442795.1:p.Ile682Val
ENST00000256993.8:c.2044A>G	ENSP00000256993.5:p.Ile682Val
ENST00000399249.6:c.2044A>G	ENSP00000382193.2:p.Ile682Val
ENST00000544791.1:c.2044A>G	ENSP00000444259.1:p.Ile682Val
ENST00000545968.5:c.2044A>G	ENSP00000442795.1:p.Ile682Val
NM_000256.3:c.2044A>G , LRG_386t1:c.2044A>G MANE Select	NP_000247.2:p.Ile682Val
XM_011520117.1:c.2026A>G	XP_011518419.1:p.Ile676Val
XM_011520118.1:c.2044A>G	XP_011518420.1:p.Ile682Val