Canonical Allele Identifier: CA021418
Gene: TNNI3 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.55156237C>A
GRCh37 chr19:g.55667605C>A
gnomAD v2:
19:55667605 C / A
gnomAD v3:
19:55156237 C / A
gnomAD v4:
chr19-55156237-C-A
Joint Max Group AF 0.00012917 (NFE)
Genomes Max Group AF 0.00007911 (NFE)
Exomes Max Group AF 0.0001289 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156237C>A , CM000681.2:g.55156237C>A GRCh38
NC_000019.9:g.55667605C>A , CM000681.1:g.55667605C>A GRCh37
NC_000019.8:g.60359417C>A NCBI36
NG_007866.2:g.6496G>T , LRG_432:g.6496G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.246G>T MANE Select ENSP00000341838.5:p.Pro82=
ENST00000665070.1:c.246G>T ENSP00000499482.1:p.Pro82=
ENST00000344887.9:c.246G>T ENSP00000341838.5:p.Pro82=
ENST00000585806.5:n.245G>T
ENST00000586669.5:n.254G>T
ENST00000587176.5:n.430G>T
ENST00000587871.1:c.865G>T
ENST00000588882.1:c.171G>T ENSP00000466729.1:p.Pro57=
ENST00000590463.1:n.418G>T
NM_000363.4:c.246G>T , LRG_432t1:c.246G>T NP_000354.4:p.Pro82=
NM_000363.5:c.246G>T MANE Select NP_000354.4:p.Pro82=
Search 100 bp 5'
Search 100 bp 3'