Canonical Allele Identifier: CA436716002
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1493388
ClinVar RCV Id: RCV001984336
dbSNP Id: rs1446625124
MyVariant Identifiers: chr3:g.169482818C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765030C>T , CM000665.2:g.169765030C>T GRCh38
NC_000003.11:g.169482818C>T , CM000665.1:g.169482818C>T GRCh37
NC_000003.10:g.170965512C>T NCBI36
NG_016363.1:g.5031G>A , LRG_347:g.5031G>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.31G>A , LRG_347t1:n.31G>A