Canonical Allele Identifier: CA436715632
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1502644
ClinVar RCV Id: RCV002022443
dbSNP Id: rs2108183190
MyVariant Identifiers: chr3:g.169482701G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764913G>C , CM000665.2:g.169764913G>C GRCh38
NC_000003.11:g.169482701G>C , CM000665.1:g.169482701G>C GRCh37
NC_000003.10:g.170965395G>C NCBI36
NG_016363.1:g.5148C>G , LRG_347:g.5148C>G

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.148C>G , LRG_347t1:n.148C>G
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