Canonical Allele Identifier: CA10582137
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 242270
ClinVar RCV Id: RCV000227788
dbSNP Id: rs777348518

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764701G>C , CM000665.2:g.169764701G>C GRCh38
NC_000003.11:g.169482489G>C , CM000665.1:g.169482489G>C GRCh37
NC_000003.10:g.170965183G>C NCBI36
NG_016363.1:g.5360C>G , LRG_347:g.5360C>G

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.360C>G , LRG_347t1:n.360C>G