Canonical Allele Identifier: CA2580069063
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 2443277
ClinVar RCV Id: RCV003151669
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764826_169764827delinsAA , CM000665.2:g.169764826_169764827delinsAA GRCh38
NC_000003.11:g.169482614_169482615delinsAA , CM000665.1:g.169482614_169482615delinsAA GRCh37
NC_000003.10:g.170965308_170965309delinsAA NCBI36
NG_016363.1:g.5234_5235delinsTT , LRG_347:g.5234_5235delinsTT

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.234_235delinsTT , LRG_347t1:n.234_235delinsTT
Search 100 bp 5'
Search 100 bp 3'