Canonical Allele Identifier: CA436715711

Gene: TERC

Linked Data

• ClinVar Variation Id: 450523
• ClinVar RCV Id: RCV000523477
• dbSNP Id: rs1553915610
• MyVariant Identifiers: chr3:g.169482721T>C (hg19) ; chr3:g.169764933T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764933T>C , CM000665.2:g.169764933T>C	GRCh38
NC_000003.11:g.169482721T>C , CM000665.1:g.169482721T>C	GRCh37
NC_000003.10:g.170965415T>C	NCBI36
NG_016363.1:g.5128A>G , LRG_347:g.5128A>G

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.128A>G , LRG_347t1:n.128A>G