Canonical Allele Identifier: CA436714969
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1361014
ClinVar RCV Id: RCV001907308
dbSNP Id: rs925088948
MyVariant Identifiers: chr3:g.169482498G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764710G>A , CM000665.2:g.169764710G>A GRCh38
NC_000003.11:g.169482498G>A , CM000665.1:g.169482498G>A GRCh37
NC_000003.10:g.170965192G>A NCBI36
NG_016363.1:g.5351C>T , LRG_347:g.5351C>T

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.351C>T , LRG_347t1:n.351C>T