Canonical Allele Identifier: CA051361
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs560901632
ExAC: 19:55668993 C / T
gnomAD v2: 19-55668993-C-T
gnomAD v3: 19-55157625-C-T
gnomAD v4: 19-55157625-C-T
MyVariant Identifiers: chr19:g.55668993C>T (hg19) chr19:g.55157625C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157625C>T , CM000681.2:g.55157625C>T GRCh38
NC_000019.9:g.55668993C>T , CM000681.1:g.55668993C>T GRCh37
NC_000019.8:g.60360805C>T NCBI36
NG_007866.2:g.5108G>A , LRG_432:g.5108G>A
NG_032759.1:g.14098G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.-36G>A MANE Select ENSP00000341838.5:n.-36G>A
ENST00000665070.1:c.-36G>A ENSP00000499482.1:n.-36G>A
ENST00000344887.9:c.-36G>A ENSP00000341838.5:n.-36G>A
ENST00000586446.1:n.108G>A
ENST00000587176.5:n.149G>A
ENST00000587871.1:c.585G>A
ENST00000590463.1:n.92G>A
NM_000363.4:c.-36G>A , LRG_432t1:c.-36G>A NP_000354.4:n.-36G>A
NM_000363.5:c.-36G>A MANE Select NP_000354.4:n.-36G>A
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