Canonical Allele Identifier: CA633870765
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs1316620307
gnomAD v2: 19-55665323-C-T
gnomAD v3: 19-55153955-C-T
gnomAD v4: 19-55153955-C-T
MyVariant Identifiers: chr19:g.55665323C>T (hg19) chr19:g.55153955C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153955C>T , CM000681.2:g.55153955C>T GRCh38
NC_000019.9:g.55665323C>T , CM000681.1:g.55665323C>T GRCh37
NC_000019.8:g.60357135C>T NCBI36
NG_007866.2:g.8778G>A , LRG_432:g.8778G>A
NG_011829.2:g.284G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+75G>A MANE Select ENSP00000341838.5:n.549+75G>A
ENST00000665070.1:c.582+75G>A ENSP00000499482.1:n.582+75G>A
ENST00000344887.9:c.549+75G>A ENSP00000341838.5:n.549+75G>A
ENST00000585806.5:n.548+75G>A
ENST00000588882.1:c.474+75G>A ENSP00000466729.1:n.474+75G>A
ENST00000589864.1:n.377+75G>A
NM_000363.4:c.549+75G>A , LRG_432t1:c.549+75G>A NP_000354.4:n.549+75G>A
NM_000363.5:c.549+75G>A MANE Select NP_000354.4:n.549+75G>A
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