Canonical Allele Identifier: CA436714876
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2444891
ClinVar RCV Id: RCV003154601
dbSNP Id: rs2108182814
MyVariant Identifiers: chr3:g.169482464C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764676C>T , CM000665.2:g.169764676C>T GRCh38
NC_000003.11:g.169482464C>T , CM000665.1:g.169482464C>T GRCh37
NC_000003.10:g.170965158C>T NCBI36
NG_016363.1:g.5385G>A , LRG_347:g.5385G>A

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.385G>A , LRG_347t1:n.385G>A