Canonical Allele Identifier: CA87624557

Gene: TERC

Linked Data

• ClinVar Variation Id: 1913090
• ClinVar RCV Id: RCV002593608
• dbSNP Id: rs1028938506
• gnomAD v3: 3-169765029-A-G
• gnomAD v4: 3-169765029-A-G
• MyVariant Identifiers: chr3:g.169482817A>G (hg19) ; chr3:g.169765029A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765029A>G , CM000665.2:g.169765029A>G	GRCh38
NC_000003.11:g.169482817A>G , CM000665.1:g.169482817A>G	GRCh37
NC_000003.10:g.170965511A>G	NCBI36
NG_016363.1:g.5032T>C , LRG_347:g.5032T>C

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.32T>C , LRG_347t1:n.32T>C