Canonical Allele Identifier: CA474217862

Gene: MYBPC3

Linked Data

• MyVariant Identifiers: chr11:g.47361295G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47339744G>T , CM000673.2:g.47339744G>T	GRCh38
NC_000011.9:g.47361295G>T , CM000673.1:g.47361295G>T	GRCh37
NC_000011.8:g.47317871G>T	NCBI36
NG_007667.1:g.17959C>A , LRG_386:g.17959C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1974C>A MANE Select	ENSP00000442795.1:p.Thr658=
ENST00000256993.8:c.1974C>A	ENSP00000256993.5:p.Thr658=
ENST00000399249.6:c.1974C>A	ENSP00000382193.2:p.Thr658=
ENST00000544791.1:c.1974C>A	ENSP00000444259.1:p.Thr658=
ENST00000545968.5:c.1974C>A	ENSP00000442795.1:p.Thr658=
NM_000256.3:c.1974C>A , LRG_386t1:c.1974C>A MANE Select	NP_000247.2:p.Thr658=
XM_011520117.1:c.1956C>A	XP_011518419.1:p.Thr652=
XM_011520118.1:c.1974C>A	XP_011518420.1:p.Thr658=