Canonical Allele Identifier: CA2343275077
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs2085727417
gnomAD v4: 19-55156127-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156127C>T , CM000681.2:g.55156127C>T GRCh38
NC_000019.9:g.55667495C>T , CM000681.1:g.55667495C>T GRCh37
NC_000019.8:g.60359307C>T NCBI36
NG_007866.2:g.6606G>A , LRG_432:g.6606G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.282+74G>A MANE Select ENSP00000341838.5:n.282+74G>A
ENST00000665070.1:c.282+74G>A ENSP00000499482.1:n.282+74G>A
ENST00000344887.9:c.282+74G>A ENSP00000341838.5:n.282+74G>A
ENST00000585806.5:n.281+74G>A
ENST00000586669.5:n.290+74G>A
ENST00000587176.5:n.466+74G>A
ENST00000587871.1:c.901+74G>A
ENST00000588882.1:c.207+74G>A ENSP00000466729.1:n.207+74G>A
ENST00000590463.1:n.454+74G>A
NM_000363.4:c.282+74G>A , LRG_432t1:c.282+74G>A NP_000354.4:n.282+74G>A
NM_000363.5:c.282+74G>A MANE Select NP_000354.4:n.282+74G>A
Search 100 bp 5'
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