Allele Registry

Canonical Allele Identifier: CA10588352

Gene: TERC HGNC NCBI

Linked Data

ClinVar RCV:

RCV000255241

ClinVar Variation:

265599

dbSNP:

886039656

MyVariant.info:

GRCh38 chr3:g.169764938_169764952del

GRCh37 chr3:g.169482726_169482740del

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764940_169764954del , CM000665.2:g.169764940_169764954del	GRCh38
NC_000003.11:g.169482728_169482742del , CM000665.1:g.169482728_169482742del	GRCh37
NC_000003.10:g.170965422_170965436del	NCBI36
NG_016363.1:g.5109_5123del , LRG_347:g.5109_5123del

Transcript Alleles

HGVS	Amino-acid Change
NR_001566.1:n.109_123del , LRG_347t1:n.109_123del

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