Canonical Allele Identifier: CA340671

Gene: TERC

Linked Data

• ClinVar Variation Id: 7320
• ClinVar RCV Id: RCV000007744
• dbSNP Id: rs199422284
• MyVariant Identifiers: chr3:g.169482441G>C (hg19) ; chr3:g.169764653G>C (hg38)
• PubMed: PMID:11574891 ; PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764653G>C , CM000665.2:g.169764653G>C	GRCh38
NC_000003.11:g.169482441G>C , CM000665.1:g.169482441G>C	GRCh37
NC_000003.10:g.170965135G>C	NCBI36
NG_016363.1:g.5408C>G , LRG_347:g.5408C>G

Transcript Alleles

HGVS	Amino-acid Change
NR_001566.1:n.408C>G , LRG_347t1:n.408C>G