Canonical Allele Identifier: CA407441649

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 853502
• ClinVar RCV Id: RCV001058322
• dbSNP Id: rs2085728001
• MyVariant Identifiers: chr19:g.55667567A>T (hg19) ; chr19:g.55156199A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156199A>T , CM000681.2:g.55156199A>T	GRCh38
NC_000019.9:g.55667567A>T , CM000681.1:g.55667567A>T	GRCh37
NC_000019.8:g.60359379A>T	NCBI36
NG_007866.2:g.6534T>A , LRG_432:g.6534T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.282+2T>A MANE Select	ENSP00000341838.5:n.282+2T>A
ENST00000665070.1:c.282+2T>A	ENSP00000499482.1:n.282+2T>A
ENST00000344887.9:c.282+2T>A	ENSP00000341838.5:n.282+2T>A
ENST00000585806.5:n.281+2T>A
ENST00000586669.5:n.290+2T>A
ENST00000587176.5:n.466+2T>A
ENST00000587871.1:c.901+2T>A
ENST00000588882.1:c.207+2T>A	ENSP00000466729.1:n.207+2T>A
ENST00000590463.1:n.454+2T>A
NM_000363.4:c.282+2T>A , LRG_432t1:c.282+2T>A	NP_000354.4:n.282+2T>A
NM_000363.5:c.282+2T>A MANE Select	NP_000354.4:n.282+2T>A