Canonical Allele Identifier: CA436715916
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2840076
ClinVar RCV Id: RCV003614539
dbSNP Id: rs1203113072
gnomAD v3: 3-169764999-T-A
gnomAD v4: 3-169764999-T-A
MyVariant Identifiers: chr3:g.169482787T>A (hg19) chr3:g.169764999T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764999T>A , CM000665.2:g.169764999T>A GRCh38
NC_000003.11:g.169482787T>A , CM000665.1:g.169482787T>A GRCh37
NC_000003.10:g.170965481T>A NCBI36
NG_016363.1:g.5062A>T , LRG_347:g.5062A>T

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.62A>T , LRG_347t1:n.62A>T
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