Canonical Allele Identifier: CA436715931

Gene: TERC

Linked Data

• ClinVar Variation Id: 1024079
• ClinVar RCV Id: RCV001324219
• dbSNP Id: rs1777964371
• gnomAD v4: 3-169765004-A-G
• MyVariant Identifiers: chr3:g.169482792A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765004A>G , CM000665.2:g.169765004A>G	GRCh38
NC_000003.11:g.169482792A>G , CM000665.1:g.169482792A>G	GRCh37
NC_000003.10:g.170965486A>G	NCBI36
NG_016363.1:g.5057T>C , LRG_347:g.5057T>C

Transcript Alleles

HGVS	Amino-acid Change
NR_001566.1:n.57T>C , LRG_347t1:n.57T>C