Canonical Allele Identifier: CA343762

Gene: TERC

Linked Data

• ClinVar Variation Id: 39290
• ClinVar RCV Id: RCV000032570
• dbSNP Id: rs199422280
• gnomAD v4: 3-169764739-C-T
• MyVariant Identifiers: chr3:g.169482527C>T (hg19) ; chr3:g.169764739C>T (hg38)
• PubMed: PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764739C>T , CM000665.2:g.169764739C>T	GRCh38
NC_000003.11:g.169482527C>T , CM000665.1:g.169482527C>T	GRCh37
NC_000003.10:g.170965221C>T	NCBI36
NG_016363.1:g.5322G>A , LRG_347:g.5322G>A

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.322G>A , LRG_347t1:n.322G>A