Canonical Allele Identifier: CA2573136776
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1428637
ClinVar RCV Id: RCV001964928
dbSNP Id: rs2108183234

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764937del , CM000665.2:g.169764937del GRCh38
NC_000003.11:g.169482725del , CM000665.1:g.169482725del GRCh37
NC_000003.10:g.170965419del NCBI36
NG_016363.1:g.5125del , LRG_347:g.5125del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.125del , LRG_347t1:n.125del