Canonical Allele Identifier: CA2696797
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1913008
ClinVar RCV Id: RCV002593550
dbSNP Id: rs772608895
ExAC: 3:169482510 C / T
gnomAD v2: 3-169482510-C-T
gnomAD v4: 3-169764722-C-T
MyVariant Identifiers: chr3:g.169482510C>T (hg19) chr3:g.169764722C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764722C>T , CM000665.2:g.169764722C>T GRCh38
NC_000003.11:g.169482510C>T , CM000665.1:g.169482510C>T GRCh37
NC_000003.10:g.170965204C>T NCBI36
NG_016363.1:g.5339G>A , LRG_347:g.5339G>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.339G>A , LRG_347t1:n.339G>A
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