Canonical Allele Identifier: CA436715838
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1061979
ClinVar RCV Id: RCV001371647
dbSNP Id: rs1560578729
MyVariant Identifiers: chr3:g.169482759G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764971G>T , CM000665.2:g.169764971G>T GRCh38
NC_000003.11:g.169482759G>T , CM000665.1:g.169482759G>T GRCh37
NC_000003.10:g.170965453G>T NCBI36
NG_016363.1:g.5090C>A , LRG_347:g.5090C>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.90C>A , LRG_347t1:n.90C>A