Canonical Allele Identifier: CA407441130

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 924790
• ClinVar RCV Id: RCV001186376
• dbSNP Id: rs397516344
• MyVariant Identifiers: chr19:g.55666174G>T (hg19) ; chr19:g.55154806G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154806G>T , CM000681.2:g.55154806G>T	GRCh38
NC_000019.9:g.55666174G>T , CM000681.1:g.55666174G>T	GRCh37
NC_000019.8:g.60357986G>T	NCBI36
NG_007866.2:g.7927C>A , LRG_432:g.7927C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.307C>A MANE Select	ENSP00000341838.5:p.Arg103Ser
ENST00000665070.1:c.307C>A	ENSP00000499482.1:p.Arg103Ser
ENST00000344887.9:c.307C>A	ENSP00000341838.5:p.Arg103Ser
ENST00000585806.5:n.306C>A
ENST00000586669.5:n.315C>A
ENST00000587176.5:n.491C>A
ENST00000587871.1:c.926C>A
ENST00000588882.1:c.232C>A	ENSP00000466729.1:p.Arg78Ser
ENST00000590463.1:n.479C>A
NM_000363.4:c.307C>A , LRG_432t1:c.307C>A	NP_000354.4:p.Arg103Ser
NM_000363.5:c.307C>A MANE Select	NP_000354.4:p.Arg103Ser