Canonical Allele Identifier: CA633906538

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 2989177
• ClinVar RCV Id: RCV003849328
• dbSNP Id: rs1461610202
• gnomAD v2: 19-55667549-G-C
• gnomAD v4: 19-55156181-G-C
• MyVariant Identifiers: chr19:g.55667549G>C (hg19) ; chr19:g.55156181G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156181G>C , CM000681.2:g.55156181G>C	GRCh38
NC_000019.9:g.55667549G>C , CM000681.1:g.55667549G>C	GRCh37
NC_000019.8:g.60359361G>C	NCBI36
NG_007866.2:g.6552C>G , LRG_432:g.6552C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.282+20C>G MANE Select	ENSP00000341838.5:n.282+20C>G
ENST00000665070.1:c.282+20C>G	ENSP00000499482.1:n.282+20C>G
ENST00000344887.9:c.282+20C>G	ENSP00000341838.5:n.282+20C>G
ENST00000585806.5:n.281+20C>G
ENST00000586669.5:n.290+20C>G
ENST00000587176.5:n.466+20C>G
ENST00000587871.1:c.901+20C>G
ENST00000588882.1:c.207+20C>G	ENSP00000466729.1:n.207+20C>G
ENST00000590463.1:n.454+20C>G
NM_000363.4:c.282+20C>G , LRG_432t1:c.282+20C>G	NP_000354.4:n.282+20C>G
NM_000363.5:c.282+20C>G MANE Select	NP_000354.4:n.282+20C>G