Canonical Allele Identifier: CA380314084

Gene: MYBPC3

Linked Data

• dbSNP Id: rs1267498373
• gnomAD v2: 11-47354771-C-T
• gnomAD v4: 11-47333220-C-T
• MyVariant Identifiers: chr11:g.47354771C>T (hg19) ; chr11:g.47333220C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47333220C>T , CM000673.2:g.47333220C>T	GRCh38
NC_000011.9:g.47354771C>T , CM000673.1:g.47354771C>T	GRCh37
NC_000011.8:g.47311347C>T	NCBI36
NG_007667.1:g.24483G>A , LRG_386:g.24483G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.3304G>A MANE Select	ENSP00000442795.1:p.Val1102Met
ENST00000256993.8:c.3304G>A	ENSP00000256993.5:p.Val1102Met
ENST00000399249.6:c.3304G>A	ENSP00000382193.2:p.Val1102Met
ENST00000545968.5:c.3304G>A	ENSP00000442795.1:p.Val1102Met
NM_000256.3:c.3304G>A , LRG_386t1:c.3304G>A MANE Select	NP_000247.2:p.Val1102Met
XM_011520117.1:c.3286G>A	XP_011518419.1:p.Val1096Met
XM_011520118.1:c.3223G>A	XP_011518420.1:p.Val1075Met