Canonical Allele Identifier: CA658822147
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 446376
ClinVar RCV Id: RCV000677349
dbSNP Id: rs1553915621

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764987_169764992dup , CM000665.2:g.169764987_169764992dup GRCh38
NC_000003.11:g.169482775_169482780dup , CM000665.1:g.169482775_169482780dup GRCh37
NC_000003.10:g.170965469_170965474dup NCBI36
NG_016363.1:g.5069_5074dup , LRG_347:g.5069_5074dup

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.69_74dup , LRG_347t1:n.69_74dup