Canonical Allele Identifier: CA343770
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 39299
ClinVar RCV Id: RCV000032579
dbSNP Id: rs199422264
MyVariant Identifiers: chr3:g.169482762_169482796del (hg19) chr3:g.169764974_169765008del (hg38)
PubMed: PMID:20301779
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764975_169765009del , CM000665.2:g.169764975_169765009del GRCh38
NC_000003.11:g.169482763_169482797del , CM000665.1:g.169482763_169482797del GRCh37
NC_000003.10:g.170965457_170965491del NCBI36
NG_016363.1:g.5053_5087del , LRG_347:g.5053_5087del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.53_87del , LRG_347t1:n.53_87del
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