Canonical Allele Identifier: CA118717

Gene: TERC

Linked Data

• ClinVar Variation Id: 7327
• ClinVar RCV Id: RCV000007751 ; RCV000032584
• dbSNP Id: rs199422268
• MyVariant Identifiers: chr3:g.169482751C>T (hg19) ; chr3:g.169764963C>T (hg38)
• PubMed: PMID:17392301 ; PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764963C>T , CM000665.2:g.169764963C>T	GRCh38
NC_000003.11:g.169482751C>T , CM000665.1:g.169482751C>T	GRCh37
NC_000003.10:g.170965445C>T	NCBI36
NG_016363.1:g.5098G>A , LRG_347:g.5098G>A

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.98G>A , LRG_347t1:n.98G>A