Canonical Allele Identifier: CA122379
Gene: TNNI2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12436
ClinVar RCV Id: RCV000013249 RCV000128665 RCV000415208
dbSNP Id: rs104894312
MyVariant Identifiers: chr11:g.1862698C>T (hg19) chr11:g.1841468C>T (hg38)
PubMed: PMID:12592607 PMID:17101001
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1841468C>T , CM000673.2:g.1841468C>T GRCh38
NC_000011.9:g.1862698C>T , CM000673.1:g.1862698C>T GRCh37
NC_000011.8:g.1819274C>T NCBI36
NG_011621.1:g.7466C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381911.6:c.466C>T MANE Select ENSP00000371336.1:p.Arg156Ter
ENST00000252898.11:c.466C>T ENSP00000252898.7:p.Arg156Ter
ENST00000381905.3:c.466C>T ENSP00000371330.3:p.Arg156Ter
ENST00000381906.5:c.466C>T ENSP00000371331.1:p.Arg156Ter
ENST00000381911.5:c.466C>T ENSP00000371336.1:p.Arg156Ter
ENST00000617947.4:c.466C>T ENSP00000481242.1:p.Arg156Ter
NM_001145829.1:c.466C>T NP_001139301.1:p.Arg156Ter
NM_001145841.1:c.466C>T NP_001139313.1:p.Arg156Ter
NM_003282.3:c.466C>T NP_003273.1:p.Arg156Ter
NM_003282.4:c.466C>T MANE Select NP_003273.1:p.Arg156Ter
NM_001145829.2:c.466C>T NP_001139301.1:p.Arg156Ter
NM_001145841.2:c.466C>T NP_001139313.1:p.Arg156Ter
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