Canonical Allele Identifier: CA2343274134
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs2085717198

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154838A>G , CM000681.2:g.55154838A>G GRCh38
NC_000019.9:g.55666206A>G , CM000681.1:g.55666206A>G GRCh37
NC_000019.8:g.60358018A>G NCBI36
NG_007866.2:g.7895T>C , LRG_432:g.7895T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.283-8T>C MANE Select ENSP00000341838.5:n.283-8T>C
ENST00000665070.1:c.283-8T>C ENSP00000499482.1:n.283-8T>C
ENST00000344887.9:c.283-8T>C ENSP00000341838.5:n.283-8T>C
ENST00000585806.5:n.282-8T>C
ENST00000586669.5:n.291-8T>C
ENST00000587176.5:n.467-8T>C
ENST00000587871.1:c.902-8T>C
ENST00000588882.1:c.208-8T>C ENSP00000466729.1:n.208-8T>C
ENST00000590463.1:n.455-8T>C
NM_000363.4:c.283-8T>C , LRG_432t1:c.283-8T>C NP_000354.4:n.283-8T>C
NM_000363.5:c.283-8T>C MANE Select NP_000354.4:n.283-8T>C