Canonical Allele Identifier: CA436715846
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039875
ClinVar RCV Id: RCV001343430
dbSNP Id: rs1777963818
MyVariant Identifiers: chr3:g.169482762G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764974G>C , CM000665.2:g.169764974G>C GRCh38
NC_000003.11:g.169482762G>C , CM000665.1:g.169482762G>C GRCh37
NC_000003.10:g.170965456G>C NCBI36
NG_016363.1:g.5087C>G , LRG_347:g.5087C>G

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.87C>G , LRG_347t1:n.87C>G