Canonical Allele Identifier: CA436715661
Gene: TERC HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.169764921C>T
GRCh37 chr3:g.169482709C>T
gnomAD v2:
3:169482709 C / T
gnomAD v3:
3:169764921 C / T
gnomAD v4:
chr3-169764921-C-T
Joint Max Group AF 0.0000326 (EAS)
Exomes Max Group AF 0.00002205 (EAS)
ClinVar RCV:
RCV000641651
ClinVar Variation:
534184
dbSNP:
1469879190
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764921C>T , CM000665.2:g.169764921C>T GRCh38
NC_000003.11:g.169482709C>T , CM000665.1:g.169482709C>T GRCh37
NC_000003.10:g.170965403C>T NCBI36
NG_016363.1:g.5140G>A , LRG_347:g.5140G>A

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.140G>A , LRG_347t1:n.140G>A
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