Canonical Allele Identifier: CA310148584
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs760068652
MyVariant Identifiers: chr19:g.55665717T>G (hg19) chr19:g.55154349T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154349T>G , CM000681.2:g.55154349T>G GRCh38
NC_000019.9:g.55665717T>G , CM000681.1:g.55665717T>G GRCh37
NC_000019.8:g.60357529T>G NCBI36
NG_007866.2:g.8384A>C , LRG_432:g.8384A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.373-143A>C MANE Select ENSP00000341838.5:n.373-143A>C
ENST00000665070.1:c.406-143A>C ENSP00000499482.1:n.406-143A>C
ENST00000344887.9:c.373-143A>C ENSP00000341838.5:n.373-143A>C
ENST00000585806.5:n.372-143A>C
ENST00000586669.5:n.381-143A>C
ENST00000587176.5:n.948A>C
ENST00000588882.1:c.298-143A>C ENSP00000466729.1:n.298-143A>C
ENST00000589864.1:n.58A>C
NM_000363.4:c.373-143A>C , LRG_432t1:c.373-143A>C NP_000354.4:n.373-143A>C
NM_000363.5:c.373-143A>C MANE Select NP_000354.4:n.373-143A>C
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