Canonical Allele Identifier: CA436715661

Gene: TERC

Linked Data

• ClinVar Variation Id: 534184
• ClinVar RCV Id: RCV000641651
• dbSNP Id: rs1469879190
• gnomAD v2: 3-169482709-C-T
• gnomAD v3: 3-169764921-C-T
• gnomAD v4: 3-169764921-C-T
• MyVariant Identifiers: chr3:g.169482709C>T (hg19) ; chr3:g.169764921C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764921C>T , CM000665.2:g.169764921C>T	GRCh38
NC_000003.11:g.169482709C>T , CM000665.1:g.169482709C>T	GRCh37
NC_000003.10:g.170965403C>T	NCBI36
NG_016363.1:g.5140G>A , LRG_347:g.5140G>A

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.140G>A , LRG_347t1:n.140G>A