Canonical Allele Identifier: CA310146208

Gene: TNNI3

Linked Data

• dbSNP Id: rs988934141
• gnomAD v3: 19-55153945-C-T
• gnomAD v4: 19-55153945-C-T
• MyVariant Identifiers: chr19:g.55665313C>T (hg19) ; chr19:g.55153945C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153945C>T , CM000681.2:g.55153945C>T	GRCh38
NC_000019.9:g.55665313C>T , CM000681.1:g.55665313C>T	GRCh37
NC_000019.8:g.60357125C>T	NCBI36
NG_007866.2:g.8788G>A , LRG_432:g.8788G>A
NG_011829.2:g.294G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.549+85G>A MANE Select	ENSP00000341838.5:n.549+85G>A
ENST00000665070.1:c.582+85G>A	ENSP00000499482.1:n.582+85G>A
ENST00000344887.9:c.549+85G>A	ENSP00000341838.5:n.549+85G>A
ENST00000585806.5:n.548+85G>A
ENST00000588882.1:c.474+85G>A	ENSP00000466729.1:n.474+85G>A
ENST00000589864.1:n.377+85G>A
NM_000363.4:c.549+85G>A , LRG_432t1:c.549+85G>A	NP_000354.4:n.549+85G>A
NM_000363.5:c.549+85G>A MANE Select	NP_000354.4:n.549+85G>A