Canonical Allele Identifier: CA051678
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs756457017
ExAC: 19:55663154 T / C
gnomAD v2: 19-55663154-T-C
gnomAD v4: 19-55151786-T-C
MyVariant Identifiers: chr19:g.55663154T>C (hg19) chr19:g.55151786T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151786T>C , CM000681.2:g.55151786T>C GRCh38
NC_000019.9:g.55663154T>C , CM000681.1:g.55663154T>C GRCh37
NC_000019.8:g.60354966T>C NCBI36
NG_007866.2:g.10947A>G , LRG_432:g.10947A>G
NG_011829.2:g.2453A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.*48A>G MANE Select ENSP00000341838.5:n.*48A>G
ENST00000665070.1:c.*48A>G ENSP00000499482.1:n.*48A>G
ENST00000344887.9:c.*48A>G ENSP00000341838.5:n.*48A>G
ENST00000585806.5:n.680A>G
ENST00000588882.1:c.*48A>G ENSP00000466729.1:n.*48A>G
ENST00000589864.1:n.509A>G
NM_000363.4:c.*48A>G , LRG_432t1:c.*48A>G NP_000354.4:n.*48A>G
NM_000363.5:c.*48A>G MANE Select NP_000354.4:n.*48A>G
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