Canonical Allele Identifier: CA407440266
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665418T>G (hg19) chr19:g.55154050T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154050T>G , CM000681.2:g.55154050T>G GRCh38
NC_000019.9:g.55665418T>G , CM000681.1:g.55665418T>G GRCh37
NC_000019.8:g.60357230T>G NCBI36
NG_007866.2:g.8683A>C , LRG_432:g.8683A>C
NG_011829.2:g.189A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.529A>C MANE Select ENSP00000341838.5:p.Lys177Gln
ENST00000665070.1:c.562A>C ENSP00000499482.1:p.Lys188Gln
ENST00000344887.9:c.529A>C ENSP00000341838.5:p.Lys177Gln
ENST00000585806.5:n.528A>C
ENST00000588882.1:c.454A>C ENSP00000466729.1:p.Lys152Gln
ENST00000589864.1:n.357A>C
NM_000363.4:c.529A>C , LRG_432t1:c.529A>C NP_000354.4:p.Lys177Gln
NM_000363.5:c.529A>C MANE Select NP_000354.4:p.Lys177Gln
Search 100 bp 5'
Search 100 bp 3'