Canonical Allele Identifier: CA009935

Gene: MYBPC3

Linked Data

• dbSNP Id: rs759627548
• gnomAD v2: 11-47364757-G-A
• gnomAD v3: 11-47343206-G-A
• gnomAD v4: 11-47343206-G-A
• MyVariant Identifiers: chr11:g.47364757G>A (hg19) ; chr11:g.47343206G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47343206G>A , CM000673.2:g.47343206G>A	GRCh38
NC_000011.9:g.47364757G>A , CM000673.1:g.47364757G>A	GRCh37
NC_000011.8:g.47321333G>A	NCBI36
NG_007667.1:g.14497C>T , LRG_386:g.14497C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1226+54C>T MANE Select	ENSP00000442795.1:n.1226+54C>T
ENST00000256993.8:c.1224-58C>T	ENSP00000256993.5:n.1224-58C>T
ENST00000399249.6:c.1226+54C>T	ENSP00000382193.2:n.1226+54C>T
ENST00000544791.1:c.1226+54C>T	ENSP00000444259.1:n.1226+54C>T
ENST00000545968.5:c.1226+54C>T	ENSP00000442795.1:n.1226+54C>T
NM_000256.3:c.1226+54C>T , LRG_386t1:c.1226+54C>T MANE Select	NP_000247.2:n.1226+54C>T
XM_011520117.1:c.1208+54C>T	XP_011518419.1:n.1208+54C>T
XM_011520118.1:c.1226+54C>T	XP_011518420.1:n.1226+54C>T