Canonical Allele Identifier: CA343766
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 39294
ClinVar RCV Id: RCV000032574
dbSNP Id: rs199422283
MyVariant Identifiers: chr3:g.169482457_169482458del (hg19) chr3:g.169764669_169764670del (hg38)
PubMed: PMID:20301779
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764671_169764672del , CM000665.2:g.169764671_169764672del GRCh38
NC_000003.11:g.169482459_169482460del , CM000665.1:g.169482459_169482460del GRCh37
NC_000003.10:g.170965153_170965154del NCBI36
NG_016363.1:g.5391_5392del , LRG_347:g.5391_5392del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.391_392del , LRG_347t1:n.391_392del
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