Canonical Allele Identifier: CA343755

Gene: TERC

Linked Data

• ClinVar Variation Id: 39283
• ClinVar RCV Id: RCV000032562
• dbSNP Id: rs199422275
• MyVariant Identifiers: chr3:g.169482671C>T (hg19) ; chr3:g.169764883C>T (hg38)
• PubMed: PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764883C>T , CM000665.2:g.169764883C>T	GRCh38
NC_000003.11:g.169482671C>T , CM000665.1:g.169482671C>T	GRCh37
NC_000003.10:g.170965365C>T	NCBI36
NG_016363.1:g.5178G>A , LRG_347:g.5178G>A

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.178G>A , LRG_347t1:n.178G>A