Canonical Allele Identifier: CA021784
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 165516
dbSNP Id: rs727503503

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154070C>T , CM000681.2:g.55154070C>T GRCh38
NC_000019.9:g.55665438C>T , CM000681.1:g.55665438C>T GRCh37
NC_000019.8:g.60357250C>T NCBI36
NG_007866.2:g.8663G>A , LRG_432:g.8663G>A
NG_011829.2:g.169G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.509G>A MANE Select ENSP00000341838.5:p.Arg170Gln
ENST00000665070.1:c.542G>A ENSP00000499482.1:p.Arg181Gln
ENST00000344887.9:c.509G>A ENSP00000341838.5:p.Arg170Gln
ENST00000585806.5:n.508G>A
ENST00000588882.1:c.434G>A ENSP00000466729.1:p.Arg145Gln
ENST00000589864.1:n.337G>A
NM_000363.4:c.509G>A , LRG_432t1:c.509G>A NP_000354.4:p.Arg170Gln
NM_000363.5:c.509G>A MANE Select NP_000354.4:p.Arg170Gln