Canonical Allele Identifier: CA436714744
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2112056
ClinVar RCV Id: RCV003034348
dbSNP Id: rs2108182738
MyVariant Identifiers: chr3:g.169482416C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764628C>T , CM000665.2:g.169764628C>T GRCh38
NC_000003.11:g.169482416C>T , CM000665.1:g.169482416C>T GRCh37
NC_000003.10:g.170965110C>T NCBI36
NG_016363.1:g.5433G>A , LRG_347:g.5433G>A

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.433G>A , LRG_347t1:n.433G>A
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