Canonical Allele Identifier: CA633870555
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs1404340031
gnomAD v2: 19-55663591-C-T
MyVariant Identifiers: chr19:g.55663591C>T (hg19) chr19:g.55152223C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55152223C>T , CM000681.2:g.55152223C>T GRCh38
NC_000019.9:g.55663591C>T , CM000681.1:g.55663591C>T GRCh37
NC_000019.8:g.60355403C>T NCBI36
NG_007866.2:g.10510G>A , LRG_432:g.10510G>A
NG_011829.2:g.2016G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.550-306G>A MANE Select ENSP00000341838.5:n.550-306G>A
ENST00000665070.1:c.583-306G>A ENSP00000499482.1:n.583-306G>A
ENST00000344887.9:c.550-306G>A ENSP00000341838.5:n.550-306G>A
ENST00000585806.5:n.549-306G>A
ENST00000588882.1:c.475-306G>A ENSP00000466729.1:n.475-306G>A
ENST00000589864.1:n.378-306G>A
NM_000363.4:c.550-306G>A , LRG_432t1:c.550-306G>A NP_000354.4:n.550-306G>A
NM_000363.5:c.550-306G>A MANE Select NP_000354.4:n.550-306G>A
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