Canonical Allele Identifier: CA436715597

Gene: TERC

Linked Data

• ClinVar Variation Id: 650938
• ClinVar RCV Id: RCV000806191
• dbSNP Id: rs1268597311
• gnomAD v2: 3-169482692-T-A
• gnomAD v3: 3-169764904-T-A
• gnomAD v4: 3-169764904-T-A
• MyVariant Identifiers: chr3:g.169482692T>A (hg19) ; chr3:g.169764904T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764904T>A , CM000665.2:g.169764904T>A	GRCh38
NC_000003.11:g.169482692T>A , CM000665.1:g.169482692T>A	GRCh37
NC_000003.10:g.170965386T>A	NCBI36
NG_016363.1:g.5157A>T , LRG_347:g.5157A>T

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.157A>T , LRG_347t1:n.157A>T