Canonical Allele Identifier: CA436715381

Gene: TERC

Linked Data

• ClinVar Variation Id: 534175
• ClinVar RCV Id: RCV000641642
• dbSNP Id: rs1553915599
• MyVariant Identifiers: chr3:g.169482632C>G (hg19) ; chr3:g.169764844C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764844C>G , CM000665.2:g.169764844C>G	GRCh38
NC_000003.11:g.169482632C>G , CM000665.1:g.169482632C>G	GRCh37
NC_000003.10:g.170965326C>G	NCBI36
NG_016363.1:g.5217G>C , LRG_347:g.5217G>C

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.217G>C , LRG_347t1:n.217G>C