Canonical Allele Identifier: CA436715126

Gene: TERC

Linked Data

• ClinVar Variation Id: 1443750
• ClinVar RCV Id: RCV001981382
• dbSNP Id: rs2108182940
• MyVariant Identifiers: chr3:g.169482553G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764765G>T , CM000665.2:g.169764765G>T	GRCh38
NC_000003.11:g.169482553G>T , CM000665.1:g.169482553G>T	GRCh37
NC_000003.10:g.170965247G>T	NCBI36
NG_016363.1:g.5296C>A , LRG_347:g.5296C>A

Transcript Alleles

HGVS	Amino-acid Change
NR_001566.1:n.296C>A , LRG_347t1:n.296C>A