Canonical Allele Identifier: CA2580069065
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2098214
ClinVar RCV Id: RCV003008403

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764947_169764948del , CM000665.2:g.169764947_169764948del GRCh38
NC_000003.11:g.169482735_169482736del , CM000665.1:g.169482735_169482736del GRCh37
NC_000003.10:g.170965429_170965430del NCBI36
NG_016363.1:g.5114_5115del , LRG_347:g.5114_5115del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.114_115del , LRG_347t1:n.114_115del