Canonical Allele Identifier: CA407441922

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 3073257
• ClinVar RCV Id: RCV004015271
• dbSNP Id: rs1205435733
• gnomAD v2: 19-55667663-C-T
• gnomAD v4: 19-55156295-C-T
• MyVariant Identifiers: chr19:g.55667663C>T (hg19) ; chr19:g.55156295C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156295C>T , CM000681.2:g.55156295C>T	GRCh38
NC_000019.9:g.55667663C>T , CM000681.1:g.55667663C>T	GRCh37
NC_000019.8:g.60359475C>T	NCBI36
NG_007866.2:g.6438G>A , LRG_432:g.6438G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.188G>A MANE Select	ENSP00000341838.5:p.Arg63Gln
ENST00000665070.1:c.188G>A	ENSP00000499482.1:p.Arg63Gln
ENST00000344887.9:c.188G>A	ENSP00000341838.5:p.Arg63Gln
ENST00000585806.5:n.187G>A
ENST00000586669.5:n.196G>A
ENST00000586858.1:c.151G>A	ENSP00000465258.1:p.Glu51Lys
ENST00000587176.5:n.372G>A
ENST00000587871.1:c.807G>A
ENST00000588882.1:c.113G>A	ENSP00000466729.1:p.Arg38Gln
ENST00000590463.1:n.360G>A
NM_000363.4:c.188G>A , LRG_432t1:c.188G>A	NP_000354.4:p.Arg63Gln
NM_000363.5:c.188G>A MANE Select	NP_000354.4:p.Arg63Gln