Canonical Allele Identifier: CA10588351
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 265266
ClinVar RCV Id: RCV000254920
dbSNP Id: rs886039437

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764680C>T , CM000665.2:g.169764680C>T GRCh38
NC_000003.11:g.169482468C>T , CM000665.1:g.169482468C>T GRCh37
NC_000003.10:g.170965162C>T NCBI36
NG_016363.1:g.5381G>A , LRG_347:g.5381G>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.381G>A , LRG_347t1:n.381G>A