Canonical Allele Identifier: CA407440203

Gene: TNNI3

Linked Data

• dbSNP Id: rs397516355
• gnomAD v2: 19-55665403-C-A
• gnomAD v4: 19-55154035-C-A
• MyVariant Identifiers: chr19:g.55665403C>A (hg19) ; chr19:g.55154035C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154035C>A , CM000681.2:g.55154035C>A	GRCh38
NC_000019.9:g.55665403C>A , CM000681.1:g.55665403C>A	GRCh37
NC_000019.8:g.60357215C>A	NCBI36
NG_007866.2:g.8698G>T , LRG_432:g.8698G>T
NG_011829.2:g.204G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.544G>T MANE Select	ENSP00000341838.5:p.Glu182Ter
ENST00000665070.1:c.577G>T	ENSP00000499482.1:p.Glu193Ter
ENST00000344887.9:c.544G>T	ENSP00000341838.5:p.Glu182Ter
ENST00000585806.5:n.543G>T
ENST00000588882.1:c.469G>T	ENSP00000466729.1:p.Glu157Ter
ENST00000589864.1:n.372G>T
NM_000363.4:c.544G>T , LRG_432t1:c.544G>T	NP_000354.4:p.Glu182Ter
NM_000363.5:c.544G>T MANE Select	NP_000354.4:p.Glu182Ter