Canonical Allele Identifier: CA87624574
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1356458
ClinVar RCV Id: RCV001876727
dbSNP Id: rs954091557
gnomAD v2: 3-169482819-C-T
gnomAD v3: 3-169765031-C-T
gnomAD v4: 3-169765031-C-T
MyVariant Identifiers: chr3:g.169482819C>T (hg19) chr3:g.169765031C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765031C>T , CM000665.2:g.169765031C>T GRCh38
NC_000003.11:g.169482819C>T , CM000665.1:g.169482819C>T GRCh37
NC_000003.10:g.170965513C>T NCBI36
NG_016363.1:g.5030G>A , LRG_347:g.5030G>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.30G>A , LRG_347t1:n.30G>A
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