Canonical Allele Identifier: CA407439656

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55151902-C-T
• MyVariant Identifiers: chr19:g.55663270C>T (hg19) ; chr19:g.55151902C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151902C>T , CM000681.2:g.55151902C>T	GRCh38
NC_000019.9:g.55663270C>T , CM000681.1:g.55663270C>T	GRCh37
NC_000019.8:g.60355082C>T	NCBI36
NG_007866.2:g.10831G>A , LRG_432:g.10831G>A
NG_011829.2:g.2337G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.565G>A MANE Select	ENSP00000341838.5:p.Gly189Arg
ENST00000665070.1:c.598G>A	ENSP00000499482.1:p.Gly200Arg
ENST00000344887.9:c.565G>A	ENSP00000341838.5:p.Gly189Arg
ENST00000585806.5:n.564G>A
ENST00000588882.1:c.490G>A	ENSP00000466729.1:p.Gly164Arg
ENST00000589864.1:n.393G>A
NM_000363.4:c.565G>A , LRG_432t1:c.565G>A	NP_000354.4:p.Gly189Arg
NM_000363.5:c.565G>A MANE Select	NP_000354.4:p.Gly189Arg