Canonical Allele Identifier: CA436716048
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 999986
ClinVar RCV Id: RCV001296057
dbSNP Id: rs1383902005
MyVariant Identifiers: chr3:g.169482836C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765048C>A , CM000665.2:g.169765048C>A GRCh38
NC_000003.11:g.169482836C>A , CM000665.1:g.169482836C>A GRCh37
NC_000003.10:g.170965530C>A NCBI36
NG_016363.1:g.5013G>T , LRG_347:g.5013G>T

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.13G>T , LRG_347t1:n.13G>T