Canonical Allele Identifier: CA436715820

Gene: TERC

Linked Data

• ClinVar Variation Id: 983511
• ClinVar RCV Id: RCV001263470 ; RCV001880061
• dbSNP Id: rs1777963668
• MyVariant Identifiers: chr3:g.169482754C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764966C>G , CM000665.2:g.169764966C>G	GRCh38
NC_000003.11:g.169482754C>G , CM000665.1:g.169482754C>G	GRCh37
NC_000003.10:g.170965448C>G	NCBI36
NG_016363.1:g.5095G>C , LRG_347:g.5095G>C

Transcript Alleles

HGVS	Amino-acid change
NR_001566.1:n.95G>C , LRG_347t1:n.95G>C