Canonical Allele Identifier: CA343771
Gene: TERC HGNC NCBI
ClinVar RCV:
RCV000032582
ClinVar Variation:
39300
dbSNP:
199422266
MyVariant.info:
GRCh38 chr3:g.169764982del
GRCh37 chr3:g.169482770del
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764982del , CM000665.2:g.169764982del GRCh38
NC_000003.11:g.169482770del , CM000665.1:g.169482770del GRCh37
NC_000003.10:g.170965464del NCBI36
NG_016363.1:g.5079del , LRG_347:g.5079del

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.79del , LRG_347t1:n.79del
Search 100 bp 5'
Search 100 bp 3'