Canonical Allele Identifier: CA436715642
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1443824
ClinVar RCV Id: RCV001981436
dbSNP Id: rs1777962706
MyVariant Identifiers: chr3:g.169482704G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764916G>A , CM000665.2:g.169764916G>A GRCh38
NC_000003.11:g.169482704G>A , CM000665.1:g.169482704G>A GRCh37
NC_000003.10:g.170965398G>A NCBI36
NG_016363.1:g.5145C>T , LRG_347:g.5145C>T

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.145C>T , LRG_347t1:n.145C>T
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