Canonical Allele Identifier: CA343752
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 39280
ClinVar RCV Id: RCV000032558
dbSNP Id: rs199422269
MyVariant Identifiers: chr3:g.169482749A>T (hg19) chr3:g.169764961A>T (hg38)
PubMed: PMID:20301779
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764961A>T , CM000665.2:g.169764961A>T GRCh38
NC_000003.11:g.169482749A>T , CM000665.1:g.169482749A>T GRCh37
NC_000003.10:g.170965443A>T NCBI36
NG_016363.1:g.5100T>A , LRG_347:g.5100T>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.100T>A , LRG_347t1:n.100T>A
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