Canonical Allele Identifier: CA343760

Gene: TERC

Linked Data

• ClinVar Variation Id: 39288
• ClinVar RCV Id: RCV000032568
• dbSNP Id: rs199422257
• MyVariant Identifiers: chr3:g.169482847C>G (hg19) ; chr3:g.169765059C>G (hg38)
• PubMed: PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765059C>G , CM000665.2:g.169765059C>G	GRCh38
NC_000003.11:g.169482847C>G , CM000665.1:g.169482847C>G	GRCh37
NC_000003.10:g.170965541C>G	NCBI36
NG_016363.1:g.5002G>C , LRG_347:g.5002G>C

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.2G>C , LRG_347t1:n.2G>C