Canonical Allele Identifier: CA436715121

Gene: TERC

Linked Data

• ClinVar Variation Id: 1493727
• ClinVar RCV Id: RCV001986700
• dbSNP Id: rs1206628752
• gnomAD v2: 3-169482552-G-A
• gnomAD v3: 3-169764764-G-A
• gnomAD v4: 3-169764764-G-A
• MyVariant Identifiers: chr3:g.169482552G>A (hg19) ; chr3:g.169764764G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764764G>A , CM000665.2:g.169764764G>A	GRCh38
NC_000003.11:g.169482552G>A , CM000665.1:g.169482552G>A	GRCh37
NC_000003.10:g.170965246G>A	NCBI36
NG_016363.1:g.5297C>T , LRG_347:g.5297C>T

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.297C>T , LRG_347t1:n.297C>T