Canonical Allele Identifier: CA436714983
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 952099
ClinVar RCV Id: RCV001224145
dbSNP Id: rs1777959711
MyVariant Identifiers: chr3:g.169482503T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764715T>A , CM000665.2:g.169764715T>A GRCh38
NC_000003.11:g.169482503T>A , CM000665.1:g.169482503T>A GRCh37
NC_000003.10:g.170965197T>A NCBI36
NG_016363.1:g.5346A>T , LRG_347:g.5346A>T

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.346A>T , LRG_347t1:n.346A>T
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