Canonical Allele Identifier: CA436715836
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2182604
ClinVar RCV Id: RCV002610935
dbSNP Id: rs1560578729
MyVariant Identifiers: chr3:g.169482759G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764971G>A , CM000665.2:g.169764971G>A GRCh38
NC_000003.11:g.169482759G>A , CM000665.1:g.169482759G>A GRCh37
NC_000003.10:g.170965453G>A NCBI36
NG_016363.1:g.5090C>T , LRG_347:g.5090C>T

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.90C>T , LRG_347t1:n.90C>T