Canonical Allele Identifier: CA2704550553
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 3014205
ClinVar RCV Id: RCV003875844
dbSNP Id: rs2108182896

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764733_169764734del , CM000665.2:g.169764733_169764734del GRCh38
NC_000003.11:g.169482521_169482522del , CM000665.1:g.169482521_169482522del GRCh37
NC_000003.10:g.170965215_170965216del NCBI36
NG_016363.1:g.5331_5332del , LRG_347:g.5331_5332del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.331_332del , LRG_347t1:n.331_332del