Canonical Allele Identifier: CA2562875729
Gene: TNNI3 HGNC NCBI

Linked Data

gnomAD v4: 19-55154292-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154292T>G , CM000681.2:g.55154292T>G GRCh38
NC_000019.9:g.55665660T>G , CM000681.1:g.55665660T>G GRCh37
NC_000019.8:g.60357472T>G NCBI36
NG_007866.2:g.8441A>C , LRG_432:g.8441A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.373-86A>C MANE Select ENSP00000341838.5:n.373-86A>C
ENST00000665070.1:c.406-86A>C ENSP00000499482.1:n.406-86A>C
ENST00000344887.9:c.373-86A>C ENSP00000341838.5:n.373-86A>C
ENST00000585806.5:n.372-86A>C
ENST00000586669.5:n.381-86A>C
ENST00000588882.1:c.298-86A>C ENSP00000466729.1:n.298-86A>C
ENST00000589864.1:n.115A>C
NM_000363.4:c.373-86A>C , LRG_432t1:c.373-86A>C NP_000354.4:n.373-86A>C
NM_000363.5:c.373-86A>C MANE Select NP_000354.4:n.373-86A>C
Search 100 bp 5'
Search 100 bp 3'