Canonical Allele Identifier: CA021896
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 181588
ClinVar RCV Id: RCV000159238
dbSNP Id: rs730881079

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151913T>C , CM000681.2:g.55151913T>C GRCh38
NC_000019.9:g.55663281T>C , CM000681.1:g.55663281T>C GRCh37
NC_000019.8:g.60355093T>C NCBI36
NG_007866.2:g.10820A>G , LRG_432:g.10820A>G
NG_011829.2:g.2326A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.554A>G MANE Select ENSP00000341838.5:p.Asn185Ser
ENST00000665070.1:c.587A>G ENSP00000499482.1:p.Asn196Ser
ENST00000344887.9:c.554A>G ENSP00000341838.5:p.Asn185Ser
ENST00000585806.5:n.553A>G
ENST00000588882.1:c.479A>G ENSP00000466729.1:p.Asn160Ser
ENST00000589864.1:n.382A>G
NM_000363.4:c.554A>G , LRG_432t1:c.554A>G NP_000354.4:p.Asn185Ser
NM_000363.5:c.554A>G MANE Select NP_000354.4:p.Asn185Ser