Canonical Allele Identifier: CA10649138

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 330198
• ClinVar RCV Id: RCV000279315 ; RCV000334316 ; RCV000387771 ; RCV000402197
• dbSNP Id: rs886054635
• gnomAD v3: 19-55151928-G-A
• gnomAD v4: 19-55151928-G-A
• MyVariant Identifiers: chr19:g.55663296G>A (hg19) ; chr19:g.55151928G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151928G>A , CM000681.2:g.55151928G>A	GRCh38
NC_000019.9:g.55663296G>A , CM000681.1:g.55663296G>A	GRCh37
NC_000019.8:g.60355108G>A	NCBI36
NG_007866.2:g.10805C>T , LRG_432:g.10805C>T
NG_011829.2:g.2311C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.550-11C>T MANE Select	ENSP00000341838.5:n.550-11C>T
ENST00000665070.1:c.583-11C>T	ENSP00000499482.1:n.583-11C>T
ENST00000344887.9:c.550-11C>T	ENSP00000341838.5:n.550-11C>T
ENST00000585806.5:n.549-11C>T
ENST00000588882.1:c.475-11C>T	ENSP00000466729.1:n.475-11C>T
ENST00000589864.1:n.378-11C>T
NM_000363.4:c.550-11C>T , LRG_432t1:c.550-11C>T	NP_000354.4:n.550-11C>T
NM_000363.5:c.550-11C>T MANE Select	NP_000354.4:n.550-11C>T