Canonical Allele Identifier: CA021797
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 181584
ClinVar RCV Id: RCV000159233
dbSNP Id: rs730881075

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154065G>C , CM000681.2:g.55154065G>C GRCh38
NC_000019.9:g.55665433G>C , CM000681.1:g.55665433G>C GRCh37
NC_000019.8:g.60357245G>C NCBI36
NG_007866.2:g.8668C>G , LRG_432:g.8668C>G
NG_011829.2:g.174C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.514C>G MANE Select ENSP00000341838.5:p.His172Asp
ENST00000665070.1:c.547C>G ENSP00000499482.1:p.His183Asp
ENST00000344887.9:c.514C>G ENSP00000341838.5:p.His172Asp
ENST00000585806.5:n.513C>G
ENST00000588882.1:c.439C>G ENSP00000466729.1:p.His147Asp
ENST00000589864.1:n.342C>G
NM_000363.4:c.514C>G , LRG_432t1:c.514C>G NP_000354.4:p.His172Asp
NM_000363.5:c.514C>G MANE Select NP_000354.4:p.His172Asp