Canonical Allele Identifier: CA658822145
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 446379
dbSNP Id: rs1553915580

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764653_169764654delinsTT , CM000665.2:g.169764653_169764654delinsTT GRCh38
NC_000003.11:g.169482441_169482442delinsTT , CM000665.1:g.169482441_169482442delinsTT GRCh37
NC_000003.10:g.170965135_170965136delinsTT NCBI36
NG_016363.1:g.5407_5408delinsAA , LRG_347:g.5407_5408delinsAA

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.407_408delinsAA , LRG_347t1:n.407_408delinsAA