Canonical Allele Identifier: CA380318625

Gene: MYBPC3

Linked Data

• gnomAD v4: 11-47337702-G-C
• MyVariant Identifiers: chr11:g.47359253G>C (hg19) ; chr11:g.47337702G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47337702G>C , CM000673.2:g.47337702G>C	GRCh38
NC_000011.9:g.47359253G>C , CM000673.1:g.47359253G>C	GRCh37
NC_000011.8:g.47315829G>C	NCBI36
NG_007667.1:g.20001C>G , LRG_386:g.20001C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000545968.6:c.2401C>G MANE Select	ENSP00000442795.1:p.Gln801Glu
ENST00000256993.8:c.2401C>G	ENSP00000256993.5:p.Gln801Glu
ENST00000399249.6:c.2401C>G	ENSP00000382193.2:p.Gln801Glu
ENST00000544791.1:c.2401C>G	ENSP00000444259.1:p.Gln801Glu
ENST00000545968.5:c.2401C>G	ENSP00000442795.1:p.Gln801Glu
NM_000256.3:c.2401C>G , LRG_386t1:c.2401C>G MANE Select	NP_000247.2:p.Gln801Glu
XM_011520117.1:c.2383C>G	XP_011518419.1:p.Gln795Glu
XM_011520118.1:c.2320C>G	XP_011518420.1:p.Gln774Glu