Canonical Allele Identifier: CA436715397
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 36953
ClinVar RCV Id: RCV000030634
dbSNP Id: rs2108183105
MyVariant Identifiers: chr3:g.169482637G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764849G>C , CM000665.2:g.169764849G>C GRCh38
NC_000003.11:g.169482637G>C , CM000665.1:g.169482637G>C GRCh37
NC_000003.10:g.170965331G>C NCBI36
NG_016363.1:g.5212C>G , LRG_347:g.5212C>G

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.212C>G , LRG_347t1:n.212C>G