Canonical Allele Identifier: CA343761
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 39289
ClinVar RCV Id: RCV000032569
dbSNP Id: rs199422279

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764756C>T , CM000665.2:g.169764756C>T GRCh38
NC_000003.11:g.169482544C>T , CM000665.1:g.169482544C>T GRCh37
NC_000003.10:g.170965238C>T NCBI36
NG_016363.1:g.5305G>A , LRG_347:g.5305G>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.305G>A , LRG_347t1:n.305G>A