Canonical Allele Identifier: CA2736114478
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs2147283034

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153850G>C , CM000681.2:g.55153850G>C GRCh38
NC_000019.9:g.55665218G>C , CM000681.1:g.55665218G>C GRCh37
NC_000019.8:g.60357030G>C NCBI36
NG_007866.2:g.8883C>G , LRG_432:g.8883C>G
NG_011829.2:g.389C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+180C>G MANE Select ENSP00000341838.5:n.549+180C>G
ENST00000665070.1:c.582+180C>G ENSP00000499482.1:n.582+180C>G
ENST00000344887.9:c.549+180C>G ENSP00000341838.5:n.549+180C>G
ENST00000585806.5:n.548+180C>G
ENST00000588882.1:c.474+180C>G ENSP00000466729.1:n.474+180C>G
ENST00000589864.1:n.377+180C>G
NM_000363.4:c.549+180C>G , LRG_432t1:c.549+180C>G NP_000354.4:n.549+180C>G
NM_000363.5:c.549+180C>G MANE Select NP_000354.4:n.549+180C>G