Canonical Allele Identifier: CA021608
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 165518
ClinVar RCV Id: RCV000152084
dbSNP Id: rs727503505
MyVariant Identifiers: chr19:g.55665546T>C (hg19) chr19:g.55154178T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154178T>C , CM000681.2:g.55154178T>C GRCh38
NC_000019.9:g.55665546T>C , CM000681.1:g.55665546T>C GRCh37
NC_000019.8:g.60357358T>C NCBI36
NG_007866.2:g.8555A>G , LRG_432:g.8555A>G
NG_011829.2:g.61A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.401A>G MANE Select ENSP00000341838.5:p.Asp134Gly
ENST00000665070.1:c.434A>G ENSP00000499482.1:p.Asp145Gly
ENST00000344887.9:c.401A>G ENSP00000341838.5:p.Asp134Gly
ENST00000585806.5:n.400A>G
ENST00000586669.5:n.409A>G
ENST00000588882.1:c.326A>G ENSP00000466729.1:p.Asp109Gly
ENST00000589864.1:n.229A>G
NM_000363.4:c.401A>G , LRG_432t1:c.401A>G NP_000354.4:p.Asp134Gly
NM_000363.5:c.401A>G MANE Select NP_000354.4:p.Asp134Gly
Search 100 bp 5'
Search 100 bp 3'