Canonical Allele Identifier: CA891843181
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 567589
ClinVar RCV Id: RCV000687723
dbSNP Id: rs1350357211
gnomAD v4: 3-169765017-C-CAA
MyVariant Identifiers: chr3:g.169482806_169482807dup (hg19) chr3:g.169765018_169765019dup (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765022_169765023dup , CM000665.2:g.169765022_169765023dup GRCh38
NC_000003.11:g.169482810_169482811dup , CM000665.1:g.169482810_169482811dup GRCh37
NC_000003.10:g.170965504_170965505dup NCBI36
NG_016363.1:g.5042_5043dup , LRG_347:g.5042_5043dup

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.42_43dup , LRG_347t1:n.42_43dup
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