Canonical Allele Identifier: CA508989469
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665548A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154180A>G , CM000681.2:g.55154180A>G GRCh38
NC_000019.9:g.55665548A>G , CM000681.1:g.55665548A>G GRCh37
NC_000019.8:g.60357360A>G NCBI36
NG_007866.2:g.8553T>C , LRG_432:g.8553T>C
NG_011829.2:g.59T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.399T>C MANE Select ENSP00000341838.5:p.Phe133=
ENST00000665070.1:c.432T>C ENSP00000499482.1:p.Phe144=
ENST00000344887.9:c.399T>C ENSP00000341838.5:p.Phe133=
ENST00000585806.5:n.398T>C
ENST00000586669.5:n.407T>C
ENST00000588882.1:c.324T>C ENSP00000466729.1:p.Phe108=
ENST00000589864.1:n.227T>C
NM_000363.4:c.399T>C , LRG_432t1:c.399T>C NP_000354.4:p.Phe133=
NM_000363.5:c.399T>C MANE Select NP_000354.4:p.Phe133=
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