Canonical Allele Identifier: CA436715690

Gene: TERC

Linked Data

• ClinVar Variation Id: 534176
• ClinVar RCV Id: RCV000641643
• dbSNP Id: rs1306157402
• gnomAD v3: 3-169764927-G-C
• gnomAD v4: 3-169764927-G-C
• MyVariant Identifiers: chr3:g.169482715G>C (hg19) ; chr3:g.169764927G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764927G>C , CM000665.2:g.169764927G>C	GRCh38
NC_000003.11:g.169482715G>C , CM000665.1:g.169482715G>C	GRCh37
NC_000003.10:g.170965409G>C	NCBI36
NG_016363.1:g.5134C>G , LRG_347:g.5134C>G

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.134C>G , LRG_347t1:n.134C>G