Canonical Allele Identifier: CA407441668
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs2085728194

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156208T>C , CM000681.2:g.55156208T>C GRCh38
NC_000019.9:g.55667576T>C , CM000681.1:g.55667576T>C GRCh37
NC_000019.8:g.60359388T>C NCBI36
NG_007866.2:g.6525A>G , LRG_432:g.6525A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.275A>G MANE Select ENSP00000341838.5:p.Glu92Gly
ENST00000665070.1:c.275A>G ENSP00000499482.1:p.Glu92Gly
ENST00000344887.9:c.275A>G ENSP00000341838.5:p.Glu92Gly
ENST00000585806.5:n.274A>G
ENST00000586669.5:n.283A>G
ENST00000587176.5:n.459A>G
ENST00000587871.1:c.894A>G
ENST00000588882.1:c.200A>G ENSP00000466729.1:p.Glu67Gly
ENST00000590463.1:n.447A>G
NM_000363.4:c.275A>G , LRG_432t1:c.275A>G NP_000354.4:p.Glu92Gly
NM_000363.5:c.275A>G MANE Select NP_000354.4:p.Glu92Gly