Canonical Allele Identifier: CA436715498
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1037204
ClinVar RCV Id: RCV001340325
dbSNP Id: rs1391283733

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764878G>A , CM000665.2:g.169764878G>A GRCh38
NC_000003.11:g.169482666G>A , CM000665.1:g.169482666G>A GRCh37
NC_000003.10:g.170965360G>A NCBI36
NG_016363.1:g.5183C>T , LRG_347:g.5183C>T

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.183C>T , LRG_347t1:n.183C>T