Canonical Allele Identifier: CA310148615

Gene: TNNI3

Linked Data

• dbSNP Id: rs12460219
• MyVariant Identifiers: chr19:g.55665767T>C (hg19) ; chr19:g.55154399T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154399T>C , CM000681.2:g.55154399T>C	GRCh38
NC_000019.9:g.55665767T>C , CM000681.1:g.55665767T>C	GRCh37
NC_000019.8:g.60357579T>C	NCBI36
NG_007866.2:g.8334A>G , LRG_432:g.8334A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.373-193A>G MANE Select	ENSP00000341838.5:n.373-193A>G
ENST00000665070.1:c.406-193A>G	ENSP00000499482.1:n.406-193A>G
ENST00000344887.9:c.373-193A>G	ENSP00000341838.5:n.373-193A>G
ENST00000585806.5:n.372-193A>G
ENST00000586669.5:n.381-193A>G
ENST00000587176.5:n.898A>G
ENST00000588882.1:c.298-193A>G	ENSP00000466729.1:n.298-193A>G
ENST00000589864.1:n.8A>G
NM_000363.4:c.373-193A>G , LRG_432t1:c.373-193A>G	NP_000354.4:n.373-193A>G
NM_000363.5:c.373-193A>G MANE Select	NP_000354.4:n.373-193A>G