Canonical Allele Identifier: CA436715373
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 579728
ClinVar RCV Id: RCV000703084
dbSNP Id: rs1277657900
gnomAD v2: 3-169482630-C-T
gnomAD v4: 3-169764842-C-T
MyVariant Identifiers: chr3:g.169482630C>T (hg19) chr3:g.169764842C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764842C>T , CM000665.2:g.169764842C>T GRCh38
NC_000003.11:g.169482630C>T , CM000665.1:g.169482630C>T GRCh37
NC_000003.10:g.170965324C>T NCBI36
NG_016363.1:g.5219G>A , LRG_347:g.5219G>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.219G>A , LRG_347t1:n.219G>A
Search 100 bp 5'
Search 100 bp 3'