Canonical Allele Identifier: CA436715130

Gene: TERC

Linked Data

• ClinVar Variation Id: 834662
• ClinVar RCV Id: RCV001035397
• gnomAD v2: 3:169482555 G / A
• MyVariant Identifiers: chr3:g.169482555G>A (hg19) ; chr3:g.169764767G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764767G>A , CM000665.2:g.169764767G>A	GRCh38
NC_000003.11:g.169482555G>A , CM000665.1:g.169482555G>A	GRCh37
NC_000003.10:g.170965249G>A	NCBI36
NG_016363.1:g.5294C>T , LRG_347:g.5294C>T

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.294C>T , LRG_347t1:n.294C>T