Canonical Allele Identifier: CA051576
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1495637
ClinVar RCV Id: RCV001991483 RCV002331591
dbSNP Id: rs532949659
ExAC: 19:55665521 G / A
gnomAD v2: 19-55665521-G-A
gnomAD v3: 19-55154153-G-A
gnomAD v4: 19-55154153-G-A
MyVariant Identifiers: chr19:g.55665521G>A (hg19) chr19:g.55154153G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154153G>A , CM000681.2:g.55154153G>A GRCh38
NC_000019.9:g.55665521G>A , CM000681.1:g.55665521G>A GRCh37
NC_000019.8:g.60357333G>A NCBI36
NG_007866.2:g.8580C>T , LRG_432:g.8580C>T
NG_011829.2:g.86C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.426C>T MANE Select ENSP00000341838.5:p.Pro142=
ENST00000665070.1:c.459C>T ENSP00000499482.1:p.Pro153=
ENST00000344887.9:c.426C>T ENSP00000341838.5:p.Pro142=
ENST00000585806.5:n.425C>T
ENST00000586669.5:n.434C>T
ENST00000588882.1:c.351C>T ENSP00000466729.1:p.Pro117=
ENST00000589864.1:n.254C>T
NM_000363.4:c.426C>T , LRG_432t1:c.426C>T NP_000354.4:p.Pro142=
NM_000363.5:c.426C>T MANE Select NP_000354.4:p.Pro142=
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