Canonical Allele Identifier: CA436715060

Gene: TERC

Linked Data

• ClinVar Variation Id: 449106
• ClinVar RCV Id: RCV000521266
• dbSNP Id: rs1553915590
• MyVariant Identifiers: chr3:g.169482530C>T (hg19) ; chr3:g.169764742C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764742C>T , CM000665.2:g.169764742C>T	GRCh38
NC_000003.11:g.169482530C>T , CM000665.1:g.169482530C>T	GRCh37
NC_000003.10:g.170965224C>T	NCBI36
NG_016363.1:g.5319G>A , LRG_347:g.5319G>A

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.319G>A , LRG_347t1:n.319G>A