Canonical Allele Identifier: CA380318782

Gene: MYBPC3

Linked Data

• gnomAD v4: 11-47337735-C-T
• MyVariant Identifiers: chr11:g.47359286C>T (hg19) ; chr11:g.47337735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47337735C>T , CM000673.2:g.47337735C>T	GRCh38
NC_000011.9:g.47359286C>T , CM000673.1:g.47359286C>T	GRCh37
NC_000011.8:g.47315862C>T	NCBI36
NG_007667.1:g.19968G>A , LRG_386:g.19968G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.2368G>A MANE Select	ENSP00000442795.1:p.Val790Ile
ENST00000256993.8:c.2368G>A	ENSP00000256993.5:p.Val790Ile
ENST00000399249.6:c.2368G>A	ENSP00000382193.2:p.Val790Ile
ENST00000544791.1:c.2368G>A	ENSP00000444259.1:p.Val790Ile
ENST00000545968.5:c.2368G>A	ENSP00000442795.1:p.Val790Ile
NM_000256.3:c.2368G>A , LRG_386t1:c.2368G>A MANE Select	NP_000247.2:p.Val790Ile
XM_011520117.1:c.2350G>A	XP_011518419.1:p.Val784Ile
XM_011520118.1:c.2287G>A	XP_011518420.1:p.Val763Ile