Canonical Allele Identifier: CA436716036
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1897164
ClinVar RCV Id: RCV002572141
gnomAD v4: 3-169765043-G-T
MyVariant Identifiers: chr3:g.169482831G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765043G>T , CM000665.2:g.169765043G>T GRCh38
NC_000003.11:g.169482831G>T , CM000665.1:g.169482831G>T GRCh37
NC_000003.10:g.170965525G>T NCBI36
NG_016363.1:g.5018C>A , LRG_347:g.5018C>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.18C>A , LRG_347t1:n.18C>A
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