Canonical Allele Identifier: CA343754

Gene: TERC

Linked Data

• ClinVar Variation Id: 39282
• ClinVar RCV Id: RCV000032561 ; RCV001610304
• dbSNP Id: rs199422274
• MyVariant Identifiers: chr3:g.169482706C>T (hg19) ; chr3:g.169764918C>T (hg38)
• PubMed: PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764918C>T , CM000665.2:g.169764918C>T	GRCh38
NC_000003.11:g.169482706C>T , CM000665.1:g.169482706C>T	GRCh37
NC_000003.10:g.170965400C>T	NCBI36
NG_016363.1:g.5143G>A , LRG_347:g.5143G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_001566.1:n.143G>A , LRG_347t1:n.143G>A