Canonical Allele Identifier: CA436715097

Gene: TERC

Linked Data

• ClinVar Variation Id: 436976
• ClinVar RCV Id: RCV000503728
• dbSNP Id: rs1553915591
• MyVariant Identifiers: chr3:g.169482543A>C (hg19) ; chr3:g.169764755A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764755A>C , CM000665.2:g.169764755A>C	GRCh38
NC_000003.11:g.169482543A>C , CM000665.1:g.169482543A>C	GRCh37
NC_000003.10:g.170965237A>C	NCBI36
NG_016363.1:g.5306T>G , LRG_347:g.5306T>G

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.306T>G , LRG_347t1:n.306T>G