Canonical Allele Identifier: CA436714743
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1695965
ClinVar RCV Id: RCV002509816
MyVariant Identifiers: chr3:g.169482416C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764628C>G , CM000665.2:g.169764628C>G GRCh38
NC_000003.11:g.169482416C>G , CM000665.1:g.169482416C>G GRCh37
NC_000003.10:g.170965110C>G NCBI36
NG_016363.1:g.5433G>C , LRG_347:g.5433G>C

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.433G>C , LRG_347t1:n.433G>C
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