Canonical Allele Identifier: CA2696788
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1498783
ClinVar RCV Id: RCV002010280
dbSNP Id: rs759566601
ExAC: 3:169482448 G / A
gnomAD v2: 3-169482448-G-A
gnomAD v4: 3-169764660-G-A
MyVariant Identifiers: chr3:g.169482448G>A (hg19) chr3:g.169764660G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764660G>A , CM000665.2:g.169764660G>A GRCh38
NC_000003.11:g.169482448G>A , CM000665.1:g.169482448G>A GRCh37
NC_000003.10:g.170965142G>A NCBI36
NG_016363.1:g.5401C>T , LRG_347:g.5401C>T

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.401C>T , LRG_347t1:n.401C>T
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