Canonical Allele Identifier: CA407440210
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665405G>C (hg19) chr19:g.55154037G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154037G>C , CM000681.2:g.55154037G>C GRCh38
NC_000019.9:g.55665405G>C , CM000681.1:g.55665405G>C GRCh37
NC_000019.8:g.60357217G>C NCBI36
NG_007866.2:g.8696C>G , LRG_432:g.8696C>G
NG_011829.2:g.202C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.542C>G MANE Select ENSP00000341838.5:p.Thr181Ser
ENST00000665070.1:c.575C>G ENSP00000499482.1:p.Thr192Ser
ENST00000344887.9:c.542C>G ENSP00000341838.5:p.Thr181Ser
ENST00000585806.5:n.541C>G
ENST00000588882.1:c.467C>G ENSP00000466729.1:p.Thr156Ser
ENST00000589864.1:n.370C>G
NM_000363.4:c.542C>G , LRG_432t1:c.542C>G NP_000354.4:p.Thr181Ser
NM_000363.5:c.542C>G MANE Select NP_000354.4:p.Thr181Ser
Search 100 bp 5'
Search 100 bp 3'