Canonical Allele Identifier: CA2573136773
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1466965
ClinVar RCV Id: RCV001990646
dbSNP Id: rs2108183111

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764855dup , CM000665.2:g.169764855dup GRCh38
NC_000003.11:g.169482643dup , CM000665.1:g.169482643dup GRCh37
NC_000003.10:g.170965337dup NCBI36
NG_016363.1:g.5209dup , LRG_347:g.5209dup

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.209dup , LRG_347t1:n.209dup