Canonical Allele Identifier: CA310146109

Gene: TNNI3

Linked Data

• dbSNP Id: rs1002459450
• gnomAD v3: 19-55153805-C-T
• gnomAD v4: 19-55153805-C-T
• MyVariant Identifiers: chr19:g.55665173C>T (hg19) ; chr19:g.55153805C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153805C>T , CM000681.2:g.55153805C>T	GRCh38
NC_000019.9:g.55665173C>T , CM000681.1:g.55665173C>T	GRCh37
NC_000019.8:g.60356985C>T	NCBI36
NG_007866.2:g.8928G>A , LRG_432:g.8928G>A
NG_011829.2:g.434G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+225G>A MANE Select	ENSP00000341838.5:n.549+225G>A
ENST00000665070.1:c.582+225G>A	ENSP00000499482.1:n.582+225G>A
ENST00000344887.9:c.549+225G>A	ENSP00000341838.5:n.549+225G>A
ENST00000585806.5:n.548+225G>A
ENST00000588882.1:c.474+225G>A	ENSP00000466729.1:n.474+225G>A
ENST00000589864.1:n.377+225G>A
NM_000363.4:c.549+225G>A , LRG_432t1:c.549+225G>A	NP_000354.4:n.549+225G>A
NM_000363.5:c.549+225G>A MANE Select	NP_000354.4:n.549+225G>A