Canonical Allele Identifier: CA2697556977
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2764141
ClinVar RCV Id: RCV003505047

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764611dup , CM000665.2:g.169764611dup GRCh38
NC_000003.11:g.169482399dup , CM000665.1:g.169482399dup GRCh37
NC_000003.10:g.170965093dup NCBI36
NG_016363.1:g.5450dup , LRG_347:g.5450dup

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.450dup , LRG_347t1:n.450dup