Canonical Allele Identifier: CA436715832
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1006855
ClinVar RCV Id: RCV001303961
dbSNP Id: rs1777963764
MyVariant Identifiers: chr3:g.169482758C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764970C>A , CM000665.2:g.169764970C>A GRCh38
NC_000003.11:g.169482758C>A , CM000665.1:g.169482758C>A GRCh37
NC_000003.10:g.170965452C>A NCBI36
NG_016363.1:g.5091G>T , LRG_347:g.5091G>T

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.91G>T , LRG_347t1:n.91G>T