Canonical Allele Identifier: CA508989405
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3231263
ClinVar RCV Id: RCV004525334
dbSNP Id: rs1262026391
gnomAD v2: 19-55665461-C-T
gnomAD v3: 19-55154093-C-T
gnomAD v4: 19-55154093-C-T
MyVariant Identifiers: chr19:g.55665461C>T (hg19) chr19:g.55154093C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154093C>T , CM000681.2:g.55154093C>T GRCh38
NC_000019.9:g.55665461C>T , CM000681.1:g.55665461C>T GRCh37
NC_000019.8:g.60357273C>T NCBI36
NG_007866.2:g.8640G>A , LRG_432:g.8640G>A
NG_011829.2:g.146G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.486G>A MANE Select ENSP00000341838.5:p.Arg162=
ENST00000665070.1:c.519G>A ENSP00000499482.1:p.Arg173=
ENST00000344887.9:c.486G>A ENSP00000341838.5:p.Arg162=
ENST00000585806.5:n.485G>A
ENST00000588882.1:c.411G>A ENSP00000466729.1:p.Arg137=
ENST00000589864.1:n.314G>A
NM_000363.4:c.486G>A , LRG_432t1:c.486G>A NP_000354.4:p.Arg162=
NM_000363.5:c.486G>A MANE Select NP_000354.4:p.Arg162=
Search 100 bp 5'
Search 100 bp 3'