Canonical Allele Identifier: CA10583862

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 237692
• ClinVar RCV Id: RCV000229066
• dbSNP Id: rs878853957
• MyVariant Identifiers: chr19:g.55663236C>T (hg19) ; chr19:g.55151868C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151868C>T , CM000681.2:g.55151868C>T	GRCh38
NC_000019.9:g.55663236C>T , CM000681.1:g.55663236C>T	GRCh37
NC_000019.8:g.60355048C>T	NCBI36
NG_007866.2:g.10865G>A , LRG_432:g.10865G>A
NG_011829.2:g.2371G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.599G>A MANE Select	ENSP00000341838.5:p.Gly200Glu
ENST00000665070.1:c.632G>A	ENSP00000499482.1:p.Gly211Glu
ENST00000344887.9:c.599G>A	ENSP00000341838.5:p.Gly200Glu
ENST00000585806.5:n.598G>A
ENST00000588882.1:c.524G>A	ENSP00000466729.1:p.Gly175Glu
ENST00000589864.1:n.427G>A
NM_000363.4:c.599G>A , LRG_432t1:c.599G>A	NP_000354.4:p.Gly200Glu
NM_000363.5:c.599G>A MANE Select	NP_000354.4:p.Gly200Glu