Canonical Allele Identifier: CA10588352

Gene: TERC

Linked Data

• ClinVar Variation Id: 265599
• ClinVar RCV Id: RCV000255241
• dbSNP Id: rs886039656
• MyVariant Identifiers: chr3:g.169482726_169482740del (hg19) ; chr3:g.169764938_169764952del (hg38)

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