Canonical Allele Identifier: CA436715414
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1011086
ClinVar RCV Id: RCV001308835
dbSNP Id: rs1445101144
gnomAD v2: 3-169482643-C-T
gnomAD v4: 3-169764855-C-T
MyVariant Identifiers: chr3:g.169482643C>T (hg19) chr3:g.169764855C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764855C>T , CM000665.2:g.169764855C>T GRCh38
NC_000003.11:g.169482643C>T , CM000665.1:g.169482643C>T GRCh37
NC_000003.10:g.170965337C>T NCBI36
NG_016363.1:g.5206G>A , LRG_347:g.5206G>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.206G>A , LRG_347t1:n.206G>A
Search 100 bp 5'
Search 100 bp 3'