Canonical Allele Identifier: CA883722739

Gene: TNNI3

Linked Data

• dbSNP Id: rs1434357889
• gnomAD v3: 19-55154380-C-G
• gnomAD v4: 19-55154380-C-G
• MyVariant Identifiers: chr19:g.55665748C>G (hg19) ; chr19:g.55154380C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154380C>G , CM000681.2:g.55154380C>G	GRCh38
NC_000019.9:g.55665748C>G , CM000681.1:g.55665748C>G	GRCh37
NC_000019.8:g.60357560C>G	NCBI36
NG_007866.2:g.8353G>C , LRG_432:g.8353G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.373-174G>C MANE Select	ENSP00000341838.5:n.373-174G>C
ENST00000665070.1:c.406-174G>C	ENSP00000499482.1:n.406-174G>C
ENST00000344887.9:c.373-174G>C	ENSP00000341838.5:n.373-174G>C
ENST00000585806.5:n.372-174G>C
ENST00000586669.5:n.381-174G>C
ENST00000587176.5:n.917G>C
ENST00000588882.1:c.298-174G>C	ENSP00000466729.1:n.298-174G>C
ENST00000589864.1:n.27G>C
NM_000363.4:c.373-174G>C , LRG_432t1:c.373-174G>C	NP_000354.4:n.373-174G>C
NM_000363.5:c.373-174G>C MANE Select	NP_000354.4:n.373-174G>C