Canonical Allele Identifier: CA407439652
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1748957
ClinVar RCV Id: RCV002347357
MyVariant Identifiers: chr19:g.55663269C>G (hg19) chr19:g.55151901C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151901C>G , CM000681.2:g.55151901C>G GRCh38
NC_000019.9:g.55663269C>G , CM000681.1:g.55663269C>G GRCh37
NC_000019.8:g.60355081C>G NCBI36
NG_007866.2:g.10832G>C , LRG_432:g.10832G>C
NG_011829.2:g.2338G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.566G>C MANE Select ENSP00000341838.5:p.Gly189Ala
ENST00000665070.1:c.599G>C ENSP00000499482.1:p.Gly200Ala
ENST00000344887.9:c.566G>C ENSP00000341838.5:p.Gly189Ala
ENST00000585806.5:n.565G>C
ENST00000588882.1:c.491G>C ENSP00000466729.1:p.Gly164Ala
ENST00000589864.1:n.394G>C
NM_000363.4:c.566G>C , LRG_432t1:c.566G>C NP_000354.4:p.Gly189Ala
NM_000363.5:c.566G>C MANE Select NP_000354.4:p.Gly189Ala
Search 100 bp 5'
Search 100 bp 3'