Canonical Allele Identifier: CA343756

Gene: TERC

Linked Data

• ClinVar Variation Id: 39284
• ClinVar RCV Id: RCV000032563
• dbSNP Id: rs199422276
• MyVariant Identifiers: chr3:g.169482669G>A (hg19) ; chr3:g.169764881G>A (hg38)
• PubMed: PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764881G>A , CM000665.2:g.169764881G>A	GRCh38
NC_000003.11:g.169482669G>A , CM000665.1:g.169482669G>A	GRCh37
NC_000003.10:g.170965363G>A	NCBI36
NG_016363.1:g.5180C>T , LRG_347:g.5180C>T

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.180C>T , LRG_347t1:n.180C>T