Canonical Allele Identifier: CA310148525

Gene: TNNI3

Linked Data

• dbSNP Id: rs980512405
• gnomAD v3: 19-55154311-C-T
• gnomAD v4: 19-55154311-C-T
• MyVariant Identifiers: chr19:g.55665679C>T (hg19) ; chr19:g.55154311C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154311C>T , CM000681.2:g.55154311C>T	GRCh38
NC_000019.9:g.55665679C>T , CM000681.1:g.55665679C>T	GRCh37
NC_000019.8:g.60357491C>T	NCBI36
NG_007866.2:g.8422G>A , LRG_432:g.8422G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.373-105G>A MANE Select	ENSP00000341838.5:n.373-105G>A
ENST00000665070.1:c.406-105G>A	ENSP00000499482.1:n.406-105G>A
ENST00000344887.9:c.373-105G>A	ENSP00000341838.5:n.373-105G>A
ENST00000585806.5:n.372-105G>A
ENST00000586669.5:n.381-105G>A
ENST00000587176.5:n.986G>A
ENST00000588882.1:c.298-105G>A	ENSP00000466729.1:n.298-105G>A
ENST00000589864.1:n.96G>A
NM_000363.4:c.373-105G>A , LRG_432t1:c.373-105G>A	NP_000354.4:n.373-105G>A
NM_000363.5:c.373-105G>A MANE Select	NP_000354.4:n.373-105G>A