Canonical Allele Identifier: CA310144932
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 629559
ClinVar RCV Id: RCV000774268
dbSNP Id: rs902161211
MyVariant Identifiers: chr19:g.55663268T>C (hg19) chr19:g.55151900T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151900T>C , CM000681.2:g.55151900T>C GRCh38
NC_000019.9:g.55663268T>C , CM000681.1:g.55663268T>C GRCh37
NC_000019.8:g.60355080T>C NCBI36
NG_007866.2:g.10833A>G , LRG_432:g.10833A>G
NG_011829.2:g.2339A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.567A>G MANE Select ENSP00000341838.5:p.Gly189=
ENST00000665070.1:c.600A>G ENSP00000499482.1:p.Gly200=
ENST00000344887.9:c.567A>G ENSP00000341838.5:p.Gly189=
ENST00000585806.5:n.566A>G
ENST00000588882.1:c.492A>G ENSP00000466729.1:p.Gly164=
ENST00000589864.1:n.395A>G
NM_000363.4:c.567A>G , LRG_432t1:c.567A>G NP_000354.4:p.Gly189=
NM_000363.5:c.567A>G MANE Select NP_000354.4:p.Gly189=
Search 100 bp 5'
Search 100 bp 3'