Canonical Allele Identifier: CA633906492

Gene: TNNI3

Linked Data

• dbSNP Id: rs1200903586
• gnomAD v2: 19-55665715-A-T
• gnomAD v3: 19-55154347-A-T
• gnomAD v4: 19-55154347-A-T
• MyVariant Identifiers: chr19:g.55665715A>T (hg19) ; chr19:g.55154347A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154347A>T , CM000681.2:g.55154347A>T	GRCh38
NC_000019.9:g.55665715A>T , CM000681.1:g.55665715A>T	GRCh37
NC_000019.8:g.60357527A>T	NCBI36
NG_007866.2:g.8386T>A , LRG_432:g.8386T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.373-141T>A MANE Select	ENSP00000341838.5:n.373-141T>A
ENST00000665070.1:c.406-141T>A	ENSP00000499482.1:n.406-141T>A
ENST00000344887.9:c.373-141T>A	ENSP00000341838.5:n.373-141T>A
ENST00000585806.5:n.372-141T>A
ENST00000586669.5:n.381-141T>A
ENST00000587176.5:n.950T>A
ENST00000588882.1:c.298-141T>A	ENSP00000466729.1:n.298-141T>A
ENST00000589864.1:n.60T>A
NM_000363.4:c.373-141T>A , LRG_432t1:c.373-141T>A	NP_000354.4:n.373-141T>A
NM_000363.5:c.373-141T>A MANE Select	NP_000354.4:n.373-141T>A