Canonical Allele Identifier: CA436715782

Gene: TERC

Linked Data

• ClinVar Variation Id: 446377
• ClinVar RCV Id: RCV000677350
• dbSNP Id: rs1553915617
• MyVariant Identifiers: chr3:g.169482742C>A (hg19) ; chr3:g.169764954C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764954C>A , CM000665.2:g.169764954C>A	GRCh38
NC_000003.11:g.169482742C>A , CM000665.1:g.169482742C>A	GRCh37
NC_000003.10:g.170965436C>A	NCBI36
NG_016363.1:g.5107G>T , LRG_347:g.5107G>T

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.107G>T , LRG_347t1:n.107G>T