Canonical Allele Identifier: CA407439399

Gene: TNNI3

Linked Data

• dbSNP Id: rs730881083
• gnomAD v2: 19-55663209-T-C
• gnomAD v4: 19-55151841-T-C
• MyVariant Identifiers: chr19:g.55663209T>C (hg19) ; chr19:g.55151841T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151841T>C , CM000681.2:g.55151841T>C	GRCh38
NC_000019.9:g.55663209T>C , CM000681.1:g.55663209T>C	GRCh37
NC_000019.8:g.60355021T>C	NCBI36
NG_007866.2:g.10892A>G , LRG_432:g.10892A>G
NG_011829.2:g.2398A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.626A>G MANE Select	ENSP00000341838.5:p.Glu209Gly
ENST00000665070.1:c.659A>G	ENSP00000499482.1:p.Glu220Gly
ENST00000344887.9:c.626A>G	ENSP00000341838.5:p.Glu209Gly
ENST00000585806.5:n.625A>G
ENST00000588882.1:c.551A>G	ENSP00000466729.1:p.Glu184Gly
ENST00000589864.1:n.454A>G
NM_000363.4:c.626A>G , LRG_432t1:c.626A>G	NP_000354.4:p.Glu209Gly
NM_000363.5:c.626A>G MANE Select	NP_000354.4:p.Glu209Gly