Canonical Allele Identifier: CA407440293
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154064T>C , CM000681.2:g.55154064T>C GRCh38
NC_000019.9:g.55665432T>C , CM000681.1:g.55665432T>C GRCh37
NC_000019.8:g.60357244T>C NCBI36
NG_007866.2:g.8669A>G , LRG_432:g.8669A>G
NG_011829.2:g.175A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.515A>G MANE Select ENSP00000341838.5:p.His172Arg
ENST00000665070.1:c.548A>G ENSP00000499482.1:p.His183Arg
ENST00000344887.9:c.515A>G ENSP00000341838.5:p.His172Arg
ENST00000585806.5:n.514A>G
ENST00000588882.1:c.440A>G ENSP00000466729.1:p.His147Arg
ENST00000589864.1:n.343A>G
NM_000363.4:c.515A>G , LRG_432t1:c.515A>G NP_000354.4:p.His172Arg
NM_000363.5:c.515A>G MANE Select NP_000354.4:p.His172Arg