Canonical Allele Identifier: CA436714714
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 436977
ClinVar RCV Id: RCV000500627
dbSNP Id: rs1553915577
MyVariant Identifiers: chr3:g.169482406G>T (hg19) chr3:g.169764618G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764618G>T , CM000665.2:g.169764618G>T GRCh38
NC_000003.11:g.169482406G>T , CM000665.1:g.169482406G>T GRCh37
NC_000003.10:g.170965100G>T NCBI36
NG_016363.1:g.5443C>A , LRG_347:g.5443C>A

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.443C>A , LRG_347t1:n.443C>A
Search 100 bp 5'
Search 100 bp 3'