Canonical Allele Identifier: CA343772
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 39301
ClinVar RCV Id: RCV000032583
dbSNP Id: rs199422267

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764964_169764965del , CM000665.2:g.169764964_169764965del GRCh38
NC_000003.11:g.169482752_169482753del , CM000665.1:g.169482752_169482753del GRCh37
NC_000003.10:g.170965446_170965447del NCBI36
NG_016363.1:g.5096_5097del , LRG_347:g.5096_5097del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.96_97del , LRG_347t1:n.96_97del