Canonical Allele Identifier: CA118716

Gene: TERC

Linked Data

• ClinVar Variation Id: 7326
• ClinVar RCV Id: RCV000007750 ; RCV000032559 ; RCV001818142 ; RCV002509148
• dbSNP Id: rs199422272
• MyVariant Identifiers: chr3:g.169482733G>A (hg19) ; chr3:g.169764945G>A (hg38)
• PubMed: PMID:14630445 ; PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764945G>A , CM000665.2:g.169764945G>A	GRCh38
NC_000003.11:g.169482733G>A , CM000665.1:g.169482733G>A	GRCh37
NC_000003.10:g.170965427G>A	NCBI36
NG_016363.1:g.5116C>T , LRG_347:g.5116C>T

Transcript Alleles

HGVS	Amino-acid Change
NR_001566.1:n.116C>T , LRG_347t1:n.116C>T