Canonical Allele Identifier: CA633870089
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs1383117157
gnomAD v2: 19-55663152-G-C
gnomAD v3: 19-55151784-G-C
gnomAD v4: 19-55151784-G-C
MyVariant Identifiers: chr19:g.55663152G>C (hg19) chr19:g.55151784G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151784G>C , CM000681.2:g.55151784G>C GRCh38
NC_000019.9:g.55663152G>C , CM000681.1:g.55663152G>C GRCh37
NC_000019.8:g.60354964G>C NCBI36
NG_007866.2:g.10949C>G , LRG_432:g.10949C>G
NG_011829.2:g.2455C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.*50C>G MANE Select ENSP00000341838.5:n.*50C>G
ENST00000665070.1:c.*50C>G ENSP00000499482.1:n.*50C>G
ENST00000344887.9:c.*50C>G ENSP00000341838.5:n.*50C>G
ENST00000585806.5:n.682C>G
ENST00000588882.1:c.*50C>G ENSP00000466729.1:n.*50C>G
ENST00000589864.1:n.511C>G
NM_000363.4:c.*50C>G , LRG_432t1:c.*50C>G NP_000354.4:n.*50C>G
NM_000363.5:c.*50C>G MANE Select NP_000354.4:n.*50C>G
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