Canonical Allele Identifier: CA1419636249
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1044504
ClinVar RCV Id: RCV001348751
dbSNP Id: rs1777957000

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764632dup , CM000665.2:g.169764632dup GRCh38
NC_000003.11:g.169482420dup , CM000665.1:g.169482420dup GRCh37
NC_000003.10:g.170965114dup NCBI36
NG_016363.1:g.5431dup , LRG_347:g.5431dup

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.431dup , LRG_347t1:n.431dup