Canonical Allele Identifier: CA436716031
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2188564
ClinVar RCV Id: RCV002620323
dbSNP Id: rs1060502987
MyVariant Identifiers: chr3:g.169482829A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765041A>C , CM000665.2:g.169765041A>C GRCh38
NC_000003.11:g.169482829A>C , CM000665.1:g.169482829A>C GRCh37
NC_000003.10:g.170965523A>C NCBI36
NG_016363.1:g.5020T>G , LRG_347:g.5020T>G

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.20T>G , LRG_347t1:n.20T>G
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