Canonical Allele Identifier: CA658799315
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 509990
ClinVar RCV Id: RCV000605118 RCV001228162
dbSNP Id: rs1210217999
gnomAD v3: 19-55156195-C-G
gnomAD v4: 19-55156195-C-G
MyVariant Identifiers: chr19:g.55667563C>G (hg19) chr19:g.55156195C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156195C>G , CM000681.2:g.55156195C>G GRCh38
NC_000019.9:g.55667563C>G , CM000681.1:g.55667563C>G GRCh37
NC_000019.8:g.60359375C>G NCBI36
NG_007866.2:g.6538G>C , LRG_432:g.6538G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.282+6G>C MANE Select ENSP00000341838.5:n.282+6G>C
ENST00000665070.1:c.282+6G>C ENSP00000499482.1:n.282+6G>C
ENST00000344887.9:c.282+6G>C ENSP00000341838.5:n.282+6G>C
ENST00000585806.5:n.281+6G>C
ENST00000586669.5:n.290+6G>C
ENST00000587176.5:n.466+6G>C
ENST00000587871.1:c.901+6G>C
ENST00000588882.1:c.207+6G>C ENSP00000466729.1:n.207+6G>C
ENST00000590463.1:n.454+6G>C
NM_000363.4:c.282+6G>C , LRG_432t1:c.282+6G>C NP_000354.4:n.282+6G>C
NM_000363.5:c.282+6G>C MANE Select NP_000354.4:n.282+6G>C
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