Canonical Allele Identifier: CA916081443
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 844738
ClinVar RCV Id: RCV001047668
dbSNP Id: rs1777963882

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764981del , CM000665.2:g.169764981del GRCh38
NC_000003.11:g.169482769del , CM000665.1:g.169482769del GRCh37
NC_000003.10:g.170965463del NCBI36
NG_016363.1:g.5083del , LRG_347:g.5083del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.83del , LRG_347t1:n.83del