Canonical Allele Identifier: CA407441961

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 926476
• ClinVar RCV Id: RCV001189077
• dbSNP Id: rs2085729410
• MyVariant Identifiers: chr19:g.55667672T>C (hg19) ; chr19:g.55156304T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156304T>C , CM000681.2:g.55156304T>C	GRCh38
NC_000019.9:g.55667672T>C , CM000681.1:g.55667672T>C	GRCh37
NC_000019.8:g.60359484T>C	NCBI36
NG_007866.2:g.6429A>G , LRG_432:g.6429A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.179A>G MANE Select	ENSP00000341838.5:p.Glu60Gly
ENST00000665070.1:c.179A>G	ENSP00000499482.1:p.Glu60Gly
ENST00000344887.9:c.179A>G	ENSP00000341838.5:p.Glu60Gly
ENST00000585806.5:n.178A>G
ENST00000586669.5:n.187A>G
ENST00000586858.1:c.142A>G	ENSP00000465258.1:p.Ser48Gly
ENST00000587176.5:n.363A>G
ENST00000587871.1:c.798A>G
ENST00000588882.1:c.104A>G	ENSP00000466729.1:p.Glu35Gly
ENST00000590463.1:n.351A>G
NM_000363.4:c.179A>G , LRG_432t1:c.179A>G	NP_000354.4:p.Glu60Gly
NM_000363.5:c.179A>G MANE Select	NP_000354.4:p.Glu60Gly