Canonical Allele Identifier: CA436715970

Gene: TERC

Linked Data

• ClinVar Variation Id: 465770
• ClinVar RCV Id: RCV000557469
• dbSNP Id: rs1553915624
• MyVariant Identifiers: chr3:g.169482806A>C (hg19) ; chr3:g.169765018A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765018A>C , CM000665.2:g.169765018A>C	GRCh38
NC_000003.11:g.169482806A>C , CM000665.1:g.169482806A>C	GRCh37
NC_000003.10:g.170965500A>C	NCBI36
NG_016363.1:g.5043T>G , LRG_347:g.5043T>G

Transcript Alleles

HGVS	Amino-acid Change
NR_001566.1:n.43T>G , LRG_347t1:n.43T>G