Canonical Allele Identifier: CA343757
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 39285
ClinVar RCV Id: RCV000032565
dbSNP Id: rs199422278

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764837_169764850del , CM000665.2:g.169764837_169764850del GRCh38
NC_000003.11:g.169482625_169482638del , CM000665.1:g.169482625_169482638del GRCh37
NC_000003.10:g.170965319_170965332del NCBI36
NG_016363.1:g.5216_5229del , LRG_347:g.5216_5229del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.216_229del , LRG_347t1:n.216_229del