Canonical Allele Identifier: CA2695199328
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2629992
ClinVar RCV Id: RCV003402070

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764952_169764988del , CM000665.2:g.169764952_169764988del GRCh38
NC_000003.11:g.169482740_169482776del , CM000665.1:g.169482740_169482776del GRCh37
NC_000003.10:g.170965434_170965470del NCBI36
NG_016363.1:g.5074_5110del , LRG_347:g.5074_5110del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.74_110del , LRG_347t1:n.74_110del