Canonical Allele Identifier: CA407439469

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 2107194
• ClinVar RCV Id: RCV003017348
• MyVariant Identifiers: chr19:g.55663227C>T (hg19) ; chr19:g.55151859C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151859C>T , CM000681.2:g.55151859C>T	GRCh38
NC_000019.9:g.55663227C>T , CM000681.1:g.55663227C>T	GRCh37
NC_000019.8:g.60355039C>T	NCBI36
NG_007866.2:g.10874G>A , LRG_432:g.10874G>A
NG_011829.2:g.2380G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.608G>A MANE Select	ENSP00000341838.5:p.Gly203Asp
ENST00000665070.1:c.641G>A	ENSP00000499482.1:p.Gly214Asp
ENST00000344887.9:c.608G>A	ENSP00000341838.5:p.Gly203Asp
ENST00000585806.5:n.607G>A
ENST00000588882.1:c.533G>A	ENSP00000466729.1:p.Gly178Asp
ENST00000589864.1:n.436G>A
NM_000363.4:c.608G>A , LRG_432t1:c.608G>A	NP_000354.4:p.Gly203Asp
NM_000363.5:c.608G>A MANE Select	NP_000354.4:p.Gly203Asp