Canonical Allele Identifier: CA508989352

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 1616902
• ClinVar RCV Id: RCV002076204
• dbSNP Id: rs1131691856
• MyVariant Identifiers: chr19:g.55663265G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151897G>A , CM000681.2:g.55151897G>A	GRCh38
NC_000019.9:g.55663265G>A , CM000681.1:g.55663265G>A	GRCh37
NC_000019.8:g.60355077G>A	NCBI36
NG_007866.2:g.10836C>T , LRG_432:g.10836C>T
NG_011829.2:g.2342C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.570C>T MANE Select	ENSP00000341838.5:p.Asp190=
ENST00000665070.1:c.603C>T	ENSP00000499482.1:p.Asp201=
ENST00000344887.9:c.570C>T	ENSP00000341838.5:p.Asp190=
ENST00000585806.5:n.569C>T
ENST00000588882.1:c.495C>T	ENSP00000466729.1:p.Asp165=
ENST00000589864.1:n.398C>T
NM_000363.4:c.570C>T , LRG_432t1:c.570C>T	NP_000354.4:p.Asp190=
NM_000363.5:c.570C>T MANE Select	NP_000354.4:p.Asp190=