Canonical Allele Identifier: CA658822146

Gene: TERC

Linked Data

• ClinVar Variation Id: 446378
• ClinVar RCV Id: RCV000677351
• dbSNP Id: rs1553915612
• MyVariant Identifiers: chr3:g.169482724_169482727del (hg19) ; chr3:g.169764936_169764939del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764940_169764943del , CM000665.2:g.169764940_169764943del	GRCh38
NC_000003.11:g.169482728_169482731del , CM000665.1:g.169482728_169482731del	GRCh37
NC_000003.10:g.170965422_170965425del	NCBI36
NG_016363.1:g.5122_5125del , LRG_347:g.5122_5125del

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.122_125del , LRG_347t1:n.122_125del