Canonical Allele Identifier: CA997261360
Gene: TNNI3 HGNC NCBI

Linked Data

gnomAD v3: 19-55153957-T-G
gnomAD v4: 19-55153957-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153957T>G , CM000681.2:g.55153957T>G GRCh38
NC_000019.9:g.55665325T>G , CM000681.1:g.55665325T>G GRCh37
NC_000019.8:g.60357137T>G NCBI36
NG_007866.2:g.8776A>C , LRG_432:g.8776A>C
NG_011829.2:g.282A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+73A>C MANE Select ENSP00000341838.5:n.549+73A>C
ENST00000665070.1:c.582+73A>C ENSP00000499482.1:n.582+73A>C
ENST00000344887.9:c.549+73A>C ENSP00000341838.5:n.549+73A>C
ENST00000585806.5:n.548+73A>C
ENST00000588882.1:c.474+73A>C ENSP00000466729.1:n.474+73A>C
ENST00000589864.1:n.377+73A>C
NM_000363.4:c.549+73A>C , LRG_432t1:c.549+73A>C NP_000354.4:n.549+73A>C
NM_000363.5:c.549+73A>C MANE Select NP_000354.4:n.549+73A>C
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