Canonical Allele Identifier: CA436715859
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2043477
ClinVar RCV Id: RCV002913025
MyVariant Identifiers: chr3:g.169482766A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764978A>G , CM000665.2:g.169764978A>G GRCh38
NC_000003.11:g.169482766A>G , CM000665.1:g.169482766A>G GRCh37
NC_000003.10:g.170965460A>G NCBI36
NG_016363.1:g.5083T>C , LRG_347:g.5083T>C

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.83T>C , LRG_347t1:n.83T>C