Canonical Allele Identifier: CA342730
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 30265
ClinVar RCV Id: RCV000023192
dbSNP Id: rs199422263
MyVariant Identifiers: chr3:g.169482792_169482795del (hg19) chr3:g.169765004_169765007del (hg38)
PubMed: PMID:20301779 PMID:22341970
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765006_169765009del , CM000665.2:g.169765006_169765009del GRCh38
NC_000003.11:g.169482794_169482797del , CM000665.1:g.169482794_169482797del GRCh37
NC_000003.10:g.170965488_170965491del NCBI36
NG_016363.1:g.5054_5057del , LRG_347:g.5054_5057del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.54_57del , LRG_347t1:n.54_57del
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