Canonical Allele Identifier: CA113852
Gene: TCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98
ClinVar RCV Id: RCV000000118
dbSNP Id: rs606231119
MyVariant Identifiers: chr22:g.31009031T>G (hg19) chr22:g.30613044T>G (hg38)
PubMed: PMID:10518276 PMID:14632784 PMID:19373259
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30613044T>G , CM000684.2:g.30613044T>G GRCh38
NC_000022.10:g.31009031T>G , CM000684.1:g.31009031T>G GRCh37
NC_000022.9:g.29339031T>G NCBI36
NG_007263.1:g.10871T>G , LRG_116:g.10871T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000471659.2:n.600T>G
ENST00000698263.1:c.427+2T>G ENSP00000513635.1:n.427+2T>G
ENST00000698264.1:n.600T>G
ENST00000698265.1:c.427+2T>G ENSP00000513636.1:n.427+2T>G
ENST00000698266.1:c.427+2T>G ENSP00000513637.1:n.427+2T>G
ENST00000698267.1:c.427+2T>G ENSP00000513638.1:n.427+2T>G
ENST00000698268.1:c.427+2T>G ENSP00000513639.1:n.427+2T>G
ENST00000698269.1:c.258-1305T>G ENSP00000513640.1:n.258-1305T>G
ENST00000698270.1:c.427+2T>G ENSP00000513641.1:n.427+2T>G
ENST00000698271.1:c.427+2T>G ENSP00000513642.1:n.427+2T>G
ENST00000698272.1:c.427+2T>G ENSP00000513643.1:n.427+2T>G
ENST00000698273.1:c.418+2T>G ENSP00000513644.1:n.418+2T>G
ENST00000215838.8:c.427+2T>G MANE Select ENSP00000215838.3:n.427+2T>G
ENST00000215838.7:c.427+2T>G ENSP00000215838.3:n.427+2T>G
ENST00000405742.7:c.415+2T>G ENSP00000385914.3:n.415+2T>G
ENST00000407817.3:c.346+83T>G ENSP00000384914.3:n.346+83T>G
ENST00000450638.5:c.352+2T>G ENSP00000394184.2:n.352+2T>G
NM_000355.3:c.427+2T>G NP_000346.2:n.427+2T>G
NM_001184726.1:c.346+83T>G NP_001171655.1:n.346+83T>G
NM_000355.4:c.427+2T>G MANE Select NP_000346.2:n.427+2T>G
NM_001184726.2:c.346+83T>G NP_001171655.1:n.346+83T>G
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