Canonical Allele Identifier: CA436715987
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1387006
ClinVar RCV Id: RCV001881734
dbSNP Id: rs1488733250
gnomAD v2: 3-169482811-A-T
gnomAD v4: 3-169765023-A-T
MyVariant Identifiers: chr3:g.169482811A>T (hg19) chr3:g.169765023A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765023A>T , CM000665.2:g.169765023A>T GRCh38
NC_000003.11:g.169482811A>T , CM000665.1:g.169482811A>T GRCh37
NC_000003.10:g.170965505A>T NCBI36
NG_016363.1:g.5038T>A , LRG_347:g.5038T>A

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.38T>A , LRG_347t1:n.38T>A
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