Canonical Allele Identifier: CA343761
Gene: TERC HGNC NCBI
ClinVar RCV:
RCV000032569
ClinVar Variation:
39289
dbSNP:
199422279
MyVariant.info:
GRCh38 chr3:g.169764756C>T
GRCh37 chr3:g.169482544C>T
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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
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