Canonical Allele Identifier: CA436714986
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2049539
ClinVar RCV Id: RCV002914065
dbSNP Id: rs2108182881
MyVariant Identifiers: chr3:g.169482504C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764716C>A , CM000665.2:g.169764716C>A GRCh38
NC_000003.11:g.169482504C>A , CM000665.1:g.169482504C>A GRCh37
NC_000003.10:g.170965198C>A NCBI36
NG_016363.1:g.5345G>T , LRG_347:g.5345G>T

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.345G>T , LRG_347t1:n.345G>T
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