Canonical Allele Identifier: CA022024
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 181603
ClinVar RCV Id: RCV000201449 RCV000225742 RCV001239093
dbSNP Id: rs730881091
gnomAD v4: 19-55151871-C-T
MyVariant Identifiers: chr19:g.55663239C>T (hg19) chr19:g.55151871C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151871C>T , CM000681.2:g.55151871C>T GRCh38
NC_000019.9:g.55663239C>T , CM000681.1:g.55663239C>T GRCh37
NC_000019.8:g.60355051C>T NCBI36
NG_007866.2:g.10862G>A , LRG_432:g.10862G>A
NG_011829.2:g.2368G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.596G>A MANE Select ENSP00000341838.5:p.Ser199Asn
ENST00000665070.1:c.629G>A ENSP00000499482.1:p.Ser210Asn
ENST00000344887.9:c.596G>A ENSP00000341838.5:p.Ser199Asn
ENST00000585806.5:n.595G>A
ENST00000588882.1:c.521G>A ENSP00000466729.1:p.Ser174Asn
ENST00000589864.1:n.424G>A
NM_000363.4:c.596G>A , LRG_432t1:c.596G>A NP_000354.4:p.Ser199Asn
NM_000363.5:c.596G>A MANE Select NP_000354.4:p.Ser199Asn
Search 100 bp 5'
Search 100 bp 3'