Canonical Allele Identifier: CA436715965

Gene: TERC

Linked Data

• ClinVar Variation Id: 2829379
• ClinVar RCV Id: RCV003613904
• dbSNP Id: rs2108183387
• MyVariant Identifiers: chr3:g.169482804A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765016A>C , CM000665.2:g.169765016A>C	GRCh38
NC_000003.11:g.169482804A>C , CM000665.1:g.169482804A>C	GRCh37
NC_000003.10:g.170965498A>C	NCBI36
NG_016363.1:g.5045T>G , LRG_347:g.5045T>G

Transcript Alleles

HGVS	Amino-acid Change
NR_001566.1:n.45T>G , LRG_347t1:n.45T>G