Canonical Allele Identifier: CA2696785

Gene: TERC

Linked Data

• ClinVar Variation Id: 410644
• ClinVar RCV Id: RCV000474479
• dbSNP Id: rs762726864
• ExAC: 3:169482434 G / A
• gnomAD v2: 3-169482434-G-A
• gnomAD v3: 3-169764646-G-A
• gnomAD v4: 3-169764646-G-A
• MyVariant Identifiers: chr3:g.169482434G>A (hg19) ; chr3:g.169764646G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764646G>A , CM000665.2:g.169764646G>A	GRCh38
NC_000003.11:g.169482434G>A , CM000665.1:g.169482434G>A	GRCh37
NC_000003.10:g.170965128G>A	NCBI36
NG_016363.1:g.5415C>T , LRG_347:g.5415C>T

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.415C>T , LRG_347t1:n.415C>T