Canonical Allele Identifier: CA407440326
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1357921
ClinVar RCV Id: RCV001863945 RCV003164089
dbSNP Id: rs727504242
gnomAD v3: 19-55154082-G-C
gnomAD v4: 19-55154082-G-C
MyVariant Identifiers: chr19:g.55665450G>C (hg19) chr19:g.55154082G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154082G>C , CM000681.2:g.55154082G>C GRCh38
NC_000019.9:g.55665450G>C , CM000681.1:g.55665450G>C GRCh37
NC_000019.8:g.60357262G>C NCBI36
NG_007866.2:g.8651C>G , LRG_432:g.8651C>G
NG_011829.2:g.157C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.497C>G MANE Select ENSP00000341838.5:p.Ser166Cys
ENST00000665070.1:c.530C>G ENSP00000499482.1:p.Ser177Cys
ENST00000344887.9:c.497C>G ENSP00000341838.5:p.Ser166Cys
ENST00000585806.5:n.496C>G
ENST00000588882.1:c.422C>G ENSP00000466729.1:p.Ser141Cys
ENST00000589864.1:n.325C>G
NM_000363.4:c.497C>G , LRG_432t1:c.497C>G NP_000354.4:p.Ser166Cys
NM_000363.5:c.497C>G MANE Select NP_000354.4:p.Ser166Cys
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