Canonical Allele Identifier: CA436715842
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1396579
ClinVar RCV Id: RCV001903054
dbSNP Id: rs2108183299
MyVariant Identifiers: chr3:g.169482761G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764973G>T , CM000665.2:g.169764973G>T GRCh38
NC_000003.11:g.169482761G>T , CM000665.1:g.169482761G>T GRCh37
NC_000003.10:g.170965455G>T NCBI36
NG_016363.1:g.5088C>A , LRG_347:g.5088C>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.88C>A , LRG_347t1:n.88C>A