Canonical Allele Identifier: CA436714740
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1348947
ClinVar RCV Id: RCV002035088
dbSNP Id: rs2108182735
MyVariant Identifiers: chr3:g.169482415C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764627C>T , CM000665.2:g.169764627C>T GRCh38
NC_000003.11:g.169482415C>T , CM000665.1:g.169482415C>T GRCh37
NC_000003.10:g.170965109C>T NCBI36
NG_016363.1:g.5434G>A , LRG_347:g.5434G>A

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.434G>A , LRG_347t1:n.434G>A
Search 100 bp 5'
Search 100 bp 3'