Canonical Allele Identifier: CA2696826
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 964174
ClinVar RCV Id: RCV001238349
dbSNP Id: rs763886920
ExAC: 3:169482805 C / T
gnomAD v2: 3-169482805-C-T
gnomAD v3: 3-169765017-C-T
gnomAD v4: 3-169765017-C-T
MyVariant Identifiers: chr3:g.169482805C>T (hg19) chr3:g.169765017C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765017C>T , CM000665.2:g.169765017C>T GRCh38
NC_000003.11:g.169482805C>T , CM000665.1:g.169482805C>T GRCh37
NC_000003.10:g.170965499C>T NCBI36
NG_016363.1:g.5044G>A , LRG_347:g.5044G>A

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.44G>A , LRG_347t1:n.44G>A
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