Canonical Allele Identifier: CA436716007

Gene: TERC

Linked Data

• ClinVar Variation Id: 534181
• ClinVar RCV Id: RCV000641648
• dbSNP Id: rs1336050074
• gnomAD v3: 3-169765032-A-T
• gnomAD v4: 3-169765032-A-T
• COSMIC: COSN2378816
• MyVariant Identifiers: chr3:g.169482820A>T (hg19) ; chr3:g.169765032A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765032A>T , CM000665.2:g.169765032A>T	GRCh38
NC_000003.11:g.169482820A>T , CM000665.1:g.169482820A>T	GRCh37
NC_000003.10:g.170965514A>T	NCBI36
NG_016363.1:g.5029T>A , LRG_347:g.5029T>A

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.29T>A , LRG_347t1:n.29T>A