Canonical Allele Identifier: CA343767
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 39295
ClinVar RCV Id: RCV000032575
dbSNP Id: rs199422286

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764651G>C , CM000665.2:g.169764651G>C GRCh38
NC_000003.11:g.169482439G>C , CM000665.1:g.169482439G>C GRCh37
NC_000003.10:g.170965133G>C NCBI36
NG_016363.1:g.5410C>G , LRG_347:g.5410C>G

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.410C>G , LRG_347t1:n.410C>G