Canonical Allele Identifier: CA436715026

Gene: TERC

Linked Data

• ClinVar Variation Id: 1478704
• ClinVar RCV Id: RCV001974312
• dbSNP Id: rs2108182899
• MyVariant Identifiers: chr3:g.169482518A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764730A>G , CM000665.2:g.169764730A>G	GRCh38
NC_000003.11:g.169482518A>G , CM000665.1:g.169482518A>G	GRCh37
NC_000003.10:g.170965212A>G	NCBI36
NG_016363.1:g.5331T>C , LRG_347:g.5331T>C

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.331T>C , LRG_347t1:n.331T>C