Canonical Allele Identifier: CA436714940
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 639725
ClinVar RCV Id: RCV000792602
dbSNP Id: rs1475263094

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764698C>G , CM000665.2:g.169764698C>G GRCh38
NC_000003.11:g.169482486C>G , CM000665.1:g.169482486C>G GRCh37
NC_000003.10:g.170965180C>G NCBI36
NG_016363.1:g.5363G>C , LRG_347:g.5363G>C

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.363G>C , LRG_347t1:n.363G>C