Canonical Allele Identifier: CA436714714

Gene: TERC

Linked Data

• ClinVar Variation Id: 436977
• ClinVar RCV Id: RCV000500627
• dbSNP Id: rs1553915577
• MyVariant Identifiers: chr3:g.169482406G>T (hg19) ; chr3:g.169764618G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764618G>T , CM000665.2:g.169764618G>T	GRCh38
NC_000003.11:g.169482406G>T , CM000665.1:g.169482406G>T	GRCh37
NC_000003.10:g.170965100G>T	NCBI36
NG_016363.1:g.5443C>A , LRG_347:g.5443C>A

Transcript Alleles

HGVS	Amino-acid Change
NR_001566.1:n.443C>A , LRG_347t1:n.443C>A