Canonical Allele Identifier: CA021810
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 180551
ClinVar RCV Id: RCV000157531
dbSNP Id: rs730880231
MyVariant Identifiers: chr19:g.55665425C>G (hg19) chr19:g.55154057C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154057C>G , CM000681.2:g.55154057C>G GRCh38
NC_000019.9:g.55665425C>G , CM000681.1:g.55665425C>G GRCh37
NC_000019.8:g.60357237C>G NCBI36
NG_007866.2:g.8676G>C , LRG_432:g.8676G>C
NG_011829.2:g.182G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.522G>C MANE Select ENSP00000341838.5:p.Lys174Asn
ENST00000665070.1:c.555G>C ENSP00000499482.1:p.Lys185Asn
ENST00000344887.9:c.522G>C ENSP00000341838.5:p.Lys174Asn
ENST00000585806.5:n.521G>C
ENST00000588882.1:c.447G>C ENSP00000466729.1:p.Lys149Asn
ENST00000589864.1:n.350G>C
NM_000363.4:c.522G>C , LRG_432t1:c.522G>C NP_000354.4:p.Lys174Asn
NM_000363.5:c.522G>C MANE Select NP_000354.4:p.Lys174Asn
Search 100 bp 5'
Search 100 bp 3'