Canonical Allele Identifier: CA2580069064
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2126177
ClinVar RCV Id: RCV003051525

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764890dup , CM000665.2:g.169764890dup GRCh38
NC_000003.11:g.169482678dup , CM000665.1:g.169482678dup GRCh37
NC_000003.10:g.170965372dup NCBI36
NG_016363.1:g.5176dup , LRG_347:g.5176dup

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.176dup , LRG_347t1:n.176dup