Canonical Allele Identifier: CA436715287
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2744221
ClinVar RCV Id: RCV003504607
MyVariant Identifiers: chr3:g.169482602G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764814G>T , CM000665.2:g.169764814G>T GRCh38
NC_000003.11:g.169482602G>T , CM000665.1:g.169482602G>T GRCh37
NC_000003.10:g.170965296G>T NCBI36
NG_016363.1:g.5247C>A , LRG_347:g.5247C>A

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.247C>A , LRG_347t1:n.247C>A
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