Canonical Allele Identifier: CA2696792
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 939334
ClinVar RCV Id: RCV001208719
dbSNP Id: rs777348518
ExAC: 3:169482489 G / T
gnomAD v4: 3-169764701-G-T
MyVariant Identifiers: chr3:g.169482489G>T (hg19) chr3:g.169764701G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764701G>T , CM000665.2:g.169764701G>T GRCh38
NC_000003.11:g.169482489G>T , CM000665.1:g.169482489G>T GRCh37
NC_000003.10:g.170965183G>T NCBI36
NG_016363.1:g.5360C>A , LRG_347:g.5360C>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.360C>A , LRG_347t1:n.360C>A
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