Canonical Allele Identifier: CA021769
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 165517
ClinVar RCV Id: RCV000152077 RCV000197009 RCV001850072
dbSNP Id: rs727503504
MyVariant Identifiers: chr19:g.55665439G>C (hg19) chr19:g.55154071G>C (hg38)
PubMed: PMID:20031618 PMID:25326637
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154071G>C , CM000681.2:g.55154071G>C GRCh38
NC_000019.9:g.55665439G>C , CM000681.1:g.55665439G>C GRCh37
NC_000019.8:g.60357251G>C NCBI36
NG_007866.2:g.8662C>G , LRG_432:g.8662C>G
NG_011829.2:g.168C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.508C>G MANE Select ENSP00000341838.5:p.Arg170Gly
ENST00000665070.1:c.541C>G ENSP00000499482.1:p.Arg181Gly
ENST00000344887.9:c.508C>G ENSP00000341838.5:p.Arg170Gly
ENST00000585806.5:n.507C>G
ENST00000588882.1:c.433C>G ENSP00000466729.1:p.Arg145Gly
ENST00000589864.1:n.336C>G
NM_000363.4:c.508C>G , LRG_432t1:c.508C>G NP_000354.4:p.Arg170Gly
NM_000363.5:c.508C>G MANE Select NP_000354.4:p.Arg170Gly
Search 100 bp 5'
Search 100 bp 3'