Canonical Allele Identifier: CA310144788
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs910940681
gnomAD v4: 19-55151802-C-T
MyVariant Identifiers: chr19:g.55663170C>T (hg19) chr19:g.55151802C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151802C>T , CM000681.2:g.55151802C>T GRCh38
NC_000019.9:g.55663170C>T , CM000681.1:g.55663170C>T GRCh37
NC_000019.8:g.60354982C>T NCBI36
NG_007866.2:g.10931G>A , LRG_432:g.10931G>A
NG_011829.2:g.2437G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.*32G>A MANE Select ENSP00000341838.5:n.*32G>A
ENST00000665070.1:c.*32G>A ENSP00000499482.1:n.*32G>A
ENST00000344887.9:c.*32G>A ENSP00000341838.5:n.*32G>A
ENST00000585806.5:n.664G>A
ENST00000588882.1:c.*32G>A ENSP00000466729.1:n.*32G>A
ENST00000589864.1:n.493G>A
NM_000363.4:c.*32G>A , LRG_432t1:c.*32G>A NP_000354.4:n.*32G>A
NM_000363.5:c.*32G>A MANE Select NP_000354.4:n.*32G>A
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