Canonical Allele Identifier: CA407440316
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 427197
ClinVar RCV Id: RCV000489372 RCV002350090
dbSNP Id: rs1085308019
gnomAD v4: 19-55154077-C-T
MyVariant Identifiers: chr19:g.55665445C>T (hg19) chr19:g.55154077C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154077C>T , CM000681.2:g.55154077C>T GRCh38
NC_000019.9:g.55665445C>T , CM000681.1:g.55665445C>T GRCh37
NC_000019.8:g.60357257C>T NCBI36
NG_007866.2:g.8656G>A , LRG_432:g.8656G>A
NG_011829.2:g.162G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.502G>A MANE Select ENSP00000341838.5:p.Asp168Asn
ENST00000665070.1:c.535G>A ENSP00000499482.1:p.Asp179Asn
ENST00000344887.9:c.502G>A ENSP00000341838.5:p.Asp168Asn
ENST00000585806.5:n.501G>A
ENST00000588882.1:c.427G>A ENSP00000466729.1:p.Asp143Asn
ENST00000589864.1:n.330G>A
NM_000363.4:c.502G>A , LRG_432t1:c.502G>A NP_000354.4:p.Asp168Asn
NM_000363.5:c.502G>A MANE Select NP_000354.4:p.Asp168Asn
Search 100 bp 5'
Search 100 bp 3'